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Placed 22/12/08  Regulatory Technical Writer/ Project Manager ~ Switzerland Our client is a Swiss pharmaceutical company based in the Basel area. They are currently actively looking for a Regulatory Technical Writer/ Project Manager to join their established Technical Operations Team. You will liaise with various technical departments to collate the information required for assigned projects and liaise with external parties to collect input on current practices and stakeholder expectations. Subsequently you will compile technical reports, documents and development reports including regulatory documents based on GMP requirements. You will also create scientific advice documents in support of meetings with regulatory agencies in Europe and North America, managing investigational new drug application dossiers for the US and Investigational Medicinal Product Dossiers for Europe. A life science graduate, fluent in German and English you will be a self starter with good organizational and communication skills. A team player, you will be able to prioritise a busy workload, be persistent and demonstrate a can do attitude. If you are interested in this position please send you CV (in English) to
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or call on 00 41 41 766 7262. Closing dates for applicants is 31st January 2009. | 
Placed 16/12/08  | The German Institute for Quality and Efficiency in Health Care (IQWiG) is seeking a Scientific Translator
Full-time position starting as soon as possible (also suitable as a part-time position)
The position is limited to 31.03.2010 (extension not excluded) IQWiG is an independent, non-government and non-profit foundation established within the framework of Germany's health care reform. The Institute is commissioned by the paramount decision-making body of the self-government of the health care system, the Federal Joint Committee, and the Federal Ministry of Health. Its responsibilities include the evidence-based assessment of drug and non-drug interventions and clinical practice guidelines. It also publishes health information for patients and the general public. More information about the Institute can be found on its website (www.iqwig.de). A position for a scientific translator is now available. The successful applicant’s primary task will be the translation of German scientific texts into English for the Institute’s website. In addition to translation work, the new colleague will support the Institute’s various departments by editing English scientific texts (journal publications, conference abstracts, etc.) and general texts, and will also function as a contact person for any queries concerning the English language. We are seeking a colleague with excellent English and German language skills who has a degree or diploma in German-English translations (or a comparable qualification) and several years of experience in the translation of scientific documents. The Institute offers excellent working conditions in an enthusiastic team, a competitive salary, and professional development opportunities. We look forward to your application, and will also consider applicants from outside Germany who would be interested in joining us in Cologne. Please send your application by 31 January 2009 to: Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen
- Personalabteilung -
Stichwort: K-01
Dillenburger Str. 27
D-51105 Köln Applications by e-mail should be sent to
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with reference to “Stellenanzeige K-01”. | |
Placed 15/12/08 |  nspm ltd
is a successful medical communications company located in Switzerland. We implement clinical and marketing projects for international customers in the pharmaceutical industry. nspm provides a complete medical writing service across a broad spectrum of therapeutic areas, with the experience and expertise of our highly qualified in-house medical writers. For our team, we are currently looking for a SENIOR MEDICAL WRITER YOUR PROFILE - University degree and higher education (PhD/MD) in medicine, natural or health sciences, or pharmacy
- English mother tongue
- At least two years editorial or medical writing experience in the pharmaceutical industry
- Computer literacy (PowerPoint/Word)
YOUR MAIN RESPONSIBILITIES - Writing and editing medical texts, including abstracts, publications and slides
- Organising scientific symposia and meetings
- A stimulating job in a dynamic multicultural team
- Swiss salary with generous social benefits
- 6 weeks holiday
If you are interested in a challenging position and working in the heart of Switzerland, please send your CV by e-mail to
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If you require further information, please call
Dr. Ian Leighton at +41 41 377 53 41
www.nspm.com
nspm ltd, Luzernerstrase 36, CH-6045 Meggen, Switzerland |
Placed 15/12/08 |  nspm ltd
is a successful medical communications company located in Switzerland. We implement clinical and marketing projects for international customers in the pharmaceutical industry. nspm provides a complete medical writing service across a broad spectrum of therapeutic areas, with the experience and expertise of our highly qualified in-house medical writers. Due to successful continued growth of nspm ltd, we are currently seeking team members for our new UK office: SENIOR MEDICAL WRITERS/
MEDICAL WRITERS
Sale, Cheshire YOUR PROFILE - University degree and higher education (PhD/MD) in medicine, natural or health sciences, or pharmacy
- Fluent written and spoken English skills
- Editorial or medical writing experience in the pharmaceutical industry
- Computer literacy (PowerPoint/Word)
YOUR MAIN RESPONSIBILITIES - Writing and editing medical texts, including abstracts, publications and slides
- Proofreading texts
- Organising scientific symposia and meetings
- A stimulating job in a friendly and innovative environment
- An experienced and highly motivated international team
- An above-average remuneration package including 6 weeks holiday
- Potential to spend time at our headquarters in Switzerland
If you are interested in a challenging position at our new UK office, please send your CV by e-mail to
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If you require further information, please call
Dr. Karen Chapman on +44 161 962 6096
www.nspm.com | 
Placed 15/12/08 | nspm ltd
is a successful medical communications company located in Switzerland. We implement clinical and marketing projects for international customers in the pharmaceutical industry. nspm provides a complete medical writing service across a broad spectrum of therapeutic areas, with the experience and expertise of our highly qualified in-house medical writers. For our team, we are currently looking for a SENIOR MEDICAL WRITER (regulatory) YOUR PROFILE - University degree and higher education (PhD/MD) in medicine, natural or health sciences, or pharmacy
- English mother tongue
- At least two years experience in writing regulatory documents
- Computer literacy (PowerPoint/Word)
YOUR MAIN RESPONSIBILITIES - Writing and editing medical texts, including
- clinical study protocols and reports
- drug submission dossiers
- manuscripts and abstracts
- slide presentations
- Organising scientific symposia and meetings
- A stimulating job in a dynamic multicultural team
- Swiss salary with generous social benefits
- 6 weeks holiday
If you are interested in a challenging position and working in the heart of Switzerland, please send your CV by e-mail to
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If you require further information, please call
Dr. Ian Leighton at +41 41 377 53 41
www.nspm.com
nspm ltd, Luzernerstrase 36, CH-6045 Meggen, Switzerland |
Placed 9/12/08  | Do you enjoy writing?
Do you have good interpersonal skills?
Can you stay focused under tight timelines? Then this may be the job for you. Trilogy Writing & Consulting GmbH is a dynamic, growing company based in Frankfurt am Main, Germany that produces regulatory documentation and scientific publications for the international pharmaceutical industry. We currently have vacancies for: - Senior Medical Writers
- Medical Writing Manager/Project Leader
Applicants for the Senior Medical Writer positions must have the following: - At least 3 years experience actively writing regulatory documents
- Diplom/Magister/Bachelors degree in science/pharmacy (PhD not necessary)
- Fluent written and spoken English skills
- An appreciation for a well written document and an eye for details
- Enjoy proactively participating on a team with diverse personalities
- Flexibility
Applicants for the Medical Writing Manager position can expect to oversee a group of up to 5 writers and write high level documents and must have all of the above and: - At least 6 years experience actively writing regulatory documents
- Overseen and written at least 2 clinical CTDs
- Proven skills in coordinating multiple projects simultaneously
- Experience in managing 2 or more people
At Trilogy Writing you will be part of a team that provides a service to clients of more than just writing. Our writers are integral parts of clinical development teams with worldwide pharmaceutical companies. We assist those teams in writing and coordinating successful documentation across a broad spectrum of therapeutic areas, whether it is for regulatory submission packages or for publication in scientific journals. As a growing company, there is room to develop with us… and your ideas will form our future together. For further insight into who we are and what we do, please look at our website. Remuneration will be appropriate for the corresponding position, with all standard German benefits. If you are interested in exploring where your own creative input can take you, contact us. For further information about the positions, feel free to call Dr. Julia Forjanic Klapproth at +4969 138 2528 11. To apply, please write in English with your CV to Dr. Julia Forjanic Klapproth at
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Placed 27/11/08 | For the safe and optimal use of human proteins
 | | We are an expanding independent, global plasma fractionation specialist and are seeking the following position for the International Clinical R&D Department located in Vienna, Austria: | | Medical Writer (f/m) | |
Responsibilties: - Preparation of clinical study reports (phase II – IV), Investigator Brochures, regulatory submissions (CTD format), responses to health authorities and manuscripts for publication
- Development and updating of templates for clinical documents in agreement with ICH and electronic submission guidelines
- Assistance in preparation and review of clinical study protocols and statistical analysis plans
- Management of document review and QC process
- Management of outsourcing of medical writing projects
- Review of work of other writers (in-house or contract) for accuracy, quality and adherence to format and style requirements
Requirements: - University degree in medicine, natural sciences or pharmacy
- 5+ years working experience in the pharmaceutical industry or in a CRO, including 3+ years writing experience
- Ability to evaluate and interpret medical research data
- Knowledge of drug development process
- Knowledge of CFR, ICH and e-CTD guidelines
- Ability to perform several tasks simultaneously without losing sight of overall objectives.
- Advanced word-processing
- Excellent command of written English and a good knowledge of statistics
If you feel qualified please send your application including a CV with a detailed description of your relevant experience: octapharma Pharmazeutika Produktionsges.m.b.H.
Oberlaaer Straße 235, 1100 Wien
Tel.: 01/610 32 – 1311 DW, zH Fr. Mag. Julia Szigeti
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www.octapharma.com | | |
Placed 24/11/08 |  Chief Medical Writer and Medical Writers at all levels – Medical Communications (London, Basel or Manchester) Competitive salary and benefits Are you an experienced writing professional seeking a new challenge? Then join the Nucleus Group… The Nucleus Group includes the medical communications agencies MediTech Media and Health Interactions, and the medical publisher International Medical Press. With over 350 employees in ten offices around the globe, we place the highest value on the scientific knowledge and expertise of our employees, which are key to the level of service we supply to our clients. The group is undergoing good growth and we are looking to strengthen and add value to our editorial teams. We are currently seeking two Chief Medical Writers with a strong background in virology or rheumatology/immunology – one for our London office and one for our Basel office. You will be responsible for managing a team of medical writers and for delivering a diverse range of high-quality scientific materials for our virology and rheumatology/immunology accounts. You will be responsible for researching specialized areas of medical science in order to write and edit text, as well as working with design and production teams to produce a range of printed and computer-based materials to meet the needs of Nucleus’ clients. The role will also involve interacting with external scientists and physicians on critical therapeutic and scientific issues. To succeed you will be qualified to PhD or MSc level, with a wealth of writing experience in a medical communications agency or pharmaceutical company. We are also seeking Medical Writers at all levels with respiratory, virology, rheumatology/immunology, neuroscience, osteoporosis, cardiometabolic or oncology experience. For Senior Medical Writers you will have 3–5 years’ relevant medical information, communications or marketing writing experience (agency or pharmaceutical), or an appropriate combination of education and experience. To find out more please go to www.nucleusholdings.org, or, to apply, please send a copy of your CV to
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Placed 10/11/08 |  | POSITION: | Director of Clinical and Regulatory
Writing | | LOCATION: | Basel, Switzerland | | TYPE: | Permanent, Full time | ARE YOU A VERY EXPERIENCED WRITING PROFESSIONAL LOOKING FOR A NEW CHALLENGE? WOULD YOU BE EXCITED BY STARTING AND GROWING A NEW BUSINESS UNIT? WOULD YOU LIKE TO BE CLOSER TO THE BUSINESS AND CLIENTS? WOULD YOU ENJOY LIVING IN A WONDERFUL INTERNATIONAL CITY CLOSE TO THE ALPS?
IF SO, PERHAPS OUR POSITION IS FOR YOU! | Position
PHOCUS is established as a provider of high quality clinical and regulatory writing services to several clients. We are appointing this new position to play a key role in the growth of this business segment and in delivering first-class service and added value in this area. The successful candidate would join a team of high calibre individuals, committed to excellence in client service. Candidate
We seek an ambitious, solution-oriented, proactive individual with a life sciences background and higher degree (PhD or MD), 5-10 years experience in a CRO or Pharma writing group, and a proven track record in delivering a range of high quality international clinical & regulatory documents in English. People management experience would be an advantage. The individual should have an excellent knowledge of the international clinical and regulatory environment and be able to: - Write, review and assure high quality of a range of clinical & regulatory documents
- Add value for clients on optimal approach, structure and content of deliverables
- Recruit, manage, motivate and ensure performance of a group of writers
- Successfully manage clients and projects to be profitable
- Assist in developing new business from existing clients and identifying new opportunities
Application
If you are ambitious and looking for a new challenge, PHOCUS would like to hear from you. Our rewarding salary package attracts the best. To apply, please write with full supporting documentation to:
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Placed 17/11/08 |  Writer/Consultant – Healthcare Consultancy
Our client, a Healthcare/Management consultancy, offers a unique blend of business skills and communications expertise to the global healthcare industry, from high-end strategic thinking and research to internal and external communications. They are currently seeking a Writer/Consultant to join their team in Cambridgeshire.
Responsibilities: - Define, document and deliver work programmes:
- explain/present company purpose and capabilities to potential and existing clients
- write discussion documents and proposals
- scope, plan and manage multi-component work programmes
- monitor resource, budget and delivery requirements
- liaise with Practice Head and Operations Director re personal workloads, programme status, resource requirements, costings and budgets
- liaise with Finance Director re programme costings and budgets, and client invoicing.
- Client account development:
- maximise new work opportunities (programme development and new leads)
- contribute to sales activities.
- Practice development:
- working with the Practice Head to develop practice offerings.
You must be an experienced communications professional with a strong medical writing background. Experience of working with a design studio on both print and multimedia projects would be a distinct advantage. Ideally you will also have some project/client management skills, although you will also receive training in this area. In return: - Excellent salary
- Good Bonus
- 25 days holiday
- Career development
Please send your CV to
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for an immediate response. For all other vacancies within medical communications please contact me on 01273 727930 to discuss |
Placed 10/11/08 | | POSITION: | Senior Medical/Scientific Writer | | LOCATION: | Basel, Switzerland | | TYPE: | Permanent, Full time | ARE YOU AN EXPERIENCED WRITER LOOKING FOR MORE EXCITEMENT & VARIETY? WOULD YOU LIKE TO JOIN A TEAM OF EXCELLENT PEOPLE? DO YOU WANT TO DELIVER WORK THAT YOU AND THE CLIENTS ARE REALLY PROUD OF? WOULD YOU ENJOY LIVING IN A WONDERFUL INTERNATIONAL CITY CLOSE TO THE ALPS?
IF SO, PERHAPS OUR POSITION IS FOR YOU! | Position
Our projects demand a range of writing skills from regulatory and clinical writing through to publications and marketing materials. The diversity of our portfolio requires our writers to research therapeutic areas, frequently outside their expertise and under pressured timelines. All writers take direct responsibility for their projects and must be confident to interact directly with clients. Candidate
We seek a dynamic and hardworking individual with a high level of medical /scientific writing expertise, combined with a creative flair for diverse forms of written communication. The ideal candidate must be independent, solution-oriented and an effective team player.
Candidates should have a degree in medicine, life sciences, or pharmacy, with at least 3 years writing experience in a CRO, medical communications agency or pharmaceutical company. Applicants must have excellent English skills, any additional languages are assets but not required. Application
If you are ambitious and vibrant, and are searching for a rewarding job where you can see the results of your work, PHOCUS would like to hear from you. Our rewarding salary package attracts the best. To apply, please write with full supporting documentation to:
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Placed 30/10/08 |  | Medical Writer (m/f)
Based near Frankfurt | www.accovion.com | | Accovion GmbH is a leading European research organization comprising clinical development, medical writing, biostatistics, statistical programming, data management and pharmacovigilance departments. Numbering over 200 staff, Accovion provides comprehensive drug development services to the pharmaceutical and biotechnology industries. We employ some of the most skilled and experienced professionals to be found anywhere in the industry, and offer a creative scientific and international environment that will allow you to develop your own skills. Our headquarters are conveniently situated in Eschborn on the outskirts of Frankfurt. The Medical Writing department is a key function within Accovion, with highly experienced medical writers involved in all aspects of clinical and regulatory documentation, closely interacting with colleagues at all levels. We offer training and mentoring programmes to new staff, and are now further expanding the group to meet the increasing demand for quality medical writing services from our clients. Projects include editing and writing (in English) of investigator brochures, clinical study protocols, reports, summaries, and manuscripts for publication. Senior writers also undertake co-ordination and planning of submission documentation, and other senior medical communication roles. Applicants must have flawless English-language skills with the ability to express medical data accurately and concisely. They will ideally have a background in life sciences including research experience and publications. Preference will be given to candidates with experience of medical writing within the pharmaceutical industry. A sound basis in German would be a considerable advantage, as would good word-processing skills. You will receive a competitive salary, bonus and benefits package to suit your qualifications. To apply, please send your curriculum vitae including the names of two references, and two samples of your written work, to: |
 | Accovion GmbH
HR-Recruiting
Helfmann-Park 10
65760 Eschborn (Germany)
Tel. +49 6196 7709-460
Fax: +49 6916 7709-119
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| | Informal enquiries to:
| Dr. Stephen de Looze
Head of Medical Writing and
Document Management
Tel.: +49 6196 7709-312
Fax: +49 6196 7709-114
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Placed 30/10/08 | |  | | | World leader in the development of breakthrough treatments. Committed to innovation. New medicines through strong science. Think what’s possible. | | | | A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance-driven people. All of which makes us one of the most rewarding employers in our field. Senior Medical Writer/
Medical Writer
Horsham, West Sussex You will write and/or edit the production of high quality clinical documentation for submission to regulatory authorities in support of marketing applications. This will involve you acting as a member of clinical trial teams, participating in the planning of analysis and data presentation to be used for study reports and acting as a documentation consultant to ensure compliance with internal company standards and external regulatory guidelines. You will also have the opportunity to develop your career as a medical writer, writing and editing | | | | | clinical CTD summary documents, co-ordinating medical writing resources for specific clinical programs, working with external vendors and helping to organise the medical writing teams for regulatory submissions. With a minimum of a life science degree (or equivalent), you will have a knowledge of clinical development and regulatory documentation and an understanding of statistics and data interpretation. You should be a team player with strong interpersonal and presentation skills, and solid written English. A background in medical writing, including experience of managing external medical writers or regulatory knowledge would also be beneficial. In return you can expect a competitive package, flexible working, flexible benefits scheme (launching January 2009) and generous relocation assistance. For more details about these and other opportunities, please visit
www.novartis.com
quoting the reference 44730BR.
| |   | www.novartis.com |
Placed 27/10/08 |  PHASE II International is a full service medical marketing agency. We are currently expanding our editorial team and welcome applications from medical writers seeking opportunities to continue their career development. Editorial Project Executive In this role, you will manage the development and writing of components of assigned accounts. This responsibility covers editorial activities from concept to delivery on single items and complete programs, including publications strategy/planning, as well as the origination and development of manuscripts, slide kits, monographs, newsletters and congress/exhibit materials. You will be confident in defining and maintaining editorial strategy and scientific quality control, as well as delivering project outputs on schedule and within budget. The role also involves management, supervision and mentoring within our editorial team. You will also contribute to new business development both through identifying opportunities to expand existing accounts and by providing input for pitches and proposals for new accounts and projects. Key responsibilities: - Project Management/Quality Control
- Account Development/Strategic Input
- Writing/Editing
- Communication
- Budgeting
Qualifications/experience: - Life sciences BSc or equivalent; higher degree is preferred
- Experience in preparing manuscripts, abstracts and presentations using trial/study reports and NDA/EMEA documentation
- Project management skills, in particular publications or medical communications programs
- Good communication/interpersonal skills and aptitude for people management
- Commercial awareness and the ability to translate this into strategies for clients’ products
- Ability to interpret data accurately
- Demonstrated ability to identify and meet client needs
- Computer literacy, familiarity with bibliographic tools
- Willingness to attend client meetings, international congresses, etc.
- Knowledge of current regulations governing pharmaceutical marketing and CME activities is useful
Editorial Assistant In this role, you will provide essential support for the editorial department and will gain experience through involvement in a variety of medical marketing projects. Key responsibilities: - Proof-reading, styling and copy-editing
- Liaison with PHASE II studio for production of typeset material including proof-reading, style, consideration of layout, colour and format issues
- Liaison with external contacts on behalf of Medical Writers and Editors
- Tracking progress of projects, providing internal and external updates
- Liaison with team members
- Support administrative tasks (e.g. data searches, reference ordering, obtaining copyright permissions, maintaining team filing systems)
- Writing projects as appropriate, e.g. biographies, minutes, correspondence, etc.
- Assist in the co-ordinating of publications
- Participation in internal/external meetings relating to ongoing projects
Qualifications/Experience: - Ability to work as part of a team and on own initiative
- Attention to detail
- Ability to multitask and prioritise tasks
- Excellent word-processing and copy-editing skills (grammar, style considerations – adherence to PHASE II house style and client’s style preferences)
- Proficient in common software (e.g. Word, PowerPoint, Excel)
- Flexibility in performing a variety of tasks – from administrative duties to more complex projects
- Scientific/medical background or interest is desirable
- Previous communications agency or healthcare company experience is an advantage
Commitment to continuing personal development is welcomed and development opportunities within the company are supported. To apply: Send a CV and covering letter to HR Director, PHASE II International, pharmawork House, Thames Mews, Portsmouth Road, Esher, Surrey, KT10 9AD United Kingdom; or electronically to
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(http://www.phase-ii.co.uk) |
Placed 16/10/08 | | | | Boehringer Ingelheim ranks among the world's 20 leading pharmaceutical corporations. Our vision drives us forward. It helps us to foster value creation through innovation in our company and to look to the future with constantly renewed commitment and ambition | | | Boehringer Ingelheim Pharma GmbH & Co. KG in Biberach is the most important research and development site of the worldwide Boehringer Ingelheim Corporation and the company’s centre for biotechnological development and manufacture. | | |  | | | | | | | | | Within the Medical Writing Group we offer a position for a Medical Writer m/f to work on a range of demanding medical, scientific, and regulatory documents such as - Clinical trial reports of our clinical studies in phases I-IV according to ICH / GCP guidelines and Boehringer Ingelheim SOPs
- Submission documents in the CTD format
- Manuscripts for medical / scientific publications
The Medical Writing Group fulfils a central service function within the international Clinical Research Department. The work comprises all steps from conception to final quality control and is embedded in a global electronic document exchange system (IDEA / Documentum). | | | The candidate should have the following qualifications: | - Graduate scientist in a life science (biology, chemistry, pharmacy, animal or human medicine) preferably at PhD-level
- At least 2 years of experience in clinical research and a basic understanding of the pharmaceutical development process
- Excellent command of English and a good knowledge of statistics
- Hands-on experience in writing and editing of medical or scientific texts
- Enjoy writing of scientific documents with great attention to detail in a wide range of therapeutic areas
- Willingness and ability to work in a team and to take over responsibilities
- Ability to convert medical / scientific data into concise easy-to-read documents
- Open-mindedness and strong organisational and communication skills
For further information please contact Dr. Thomas Schindler, phone + 49 (0) 73 51 / 54 922 92. | | | | If you feel qualified please send your application including a detailed resume and a cover letter, describing your research experience. | | | As a company without barriers, we also welcome applications from the severely disabled if they have the relevant qualifications. | | | | Boehringer Ingelheim Pharma GmbH & Co. KG A Personalmanagement Wolfgang Groß 88397 Biberach an der Riss Germany Phone +49 (0) 73 51 / 54 44 06 | | | | | |
Placed 6/10/08  | Are you looking for an exciting new challenge and the right opportunity? Join the Envision Pharma team – we have clients across the globe and offices in the UK and USA. With a range of unique scientific and cuttingedge technology solutions including Datavision, we are market leaders in medical communications. Due to significant expansion we have opportunities for medical writers and scientific team leads which offer exciting challenges in a scientifically stimulating environment. Ideally, you will have worked in medical communications and have a relevant higher degree (or equivalent). A proven track record of medical writing and editing, plus an exceptional eye for detail are essential. As a medical writer/scientific team lead you will (depending on level of experience) demonstrate excellent writing and quality control, serve as key client/author liaison, champion key therapeutic areas, be responsible for managing your projects and successfully delivering outputs, instruct/ mentor other medical writers, and have an appreciation of the nuances of publication planning, strategy and implementation. Yes, you will be conversant with the many and varied tasks of a scientific, medical communication professional. We are a dynamic and rewarding company to work for, with excellent benefits and an informal, friendly, and vibrant work environment. Please email your CV to
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or alternatively visit www.envisionpharma.com for the latest career opportunities.
 | |
Placed 2/10/08 | Clinical Editor 12-month Contracts · £Competitive + benefits · Central London This is a great opportunity for two doctors or pharmacists to move out of practice for a year or possibly longer, joining us as Clinical Editors on our BMJ Order sets product. You will be responsible for editing and planning content for our BMJ Order sets product, working with colleagues and expert authors to develop structure and agree coverage. Orders must provide clear concise guidance to aid clinical practice and be supported by best current evidence. Combining a degree in Medicine or Pharmacy with post graduate clinical experience, you’ll have fluent written and spoken English, Microsoft Office, scientific and analytical skills. Proactive, flexible and mentally agile, you’ll demonstrate strong critical thinking, attention to detail and the ability to apply evidence-based concepts to reality. Clearly, experience of online editing or writing for a medical publication and an understanding of evidence-based medicine would be an advantage. For more information on these roles and the BMJ Group in general, please visit www.group.bmj.com/jobs To discuss the roles further, please email
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Editor, Clinical Evidence and Best Practice. To apply, email
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Placed 28/09/08 |  Meridian Healthcomms is an established and expanding medical communications agency working with high-profile clients in the pharmaceutical industry. We pride ourselves on our consistently high standards in scientific and editorial quality, our professional and experienced account management, and our proactive and creative approach to meeting communications objectives. We are seeking a Medical Writer with experience in the oncology, immunology or respiratory therapy areas for our expanding editorial team. The position is based in our offices in Cheshire, UK. The ideal writer will have a PhD in a relevant discipline and 1 to 2 years’ medical writing experience in the pharmaceutical industry or a medical communications agency. The right person should relish the prospect of a high-profile, client-facing role, and the opportunity to manage and deliver communications outputs ranging from abstracts, slide presentations and posters to manuscripts, educational materials, advisory boards and symposia. In return for your commitment to excellence, we offer a competitive salary package and a fun, friendly working environment. To apply, please email your curriculum vitae and a covering letter to Emma Hatt at Meridian HealthComms
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or phone 01606 841842 for more information. |
Placed 24/09/08 |  nspm ltd
is a successful medical communications company located in Switzerland. We implement clinical and marketing projects for international customers in the pharmaceutical industry. nspm provides a complete medical writing service across a broad spectrum of therapeutic areas, with the experience and expertise of our highly qualified in-house medical writers. For our various teams
we are currently looking for MEDICAL WRITERS YOUR PROFILE - University degree and higher education (PhD/MD) in medicine, natural or health sciences, or pharmacy
- English mother tongue
- Editorial or medical writing experience in the pharmaceutical industry is desirable
- Computer literacy (PowerPoint/Word)
YOUR MAIN RESPONSIBILITIES - Writing and editing medical texts, including abstracts, publications and slides
- Proofreading texts
- Organising scientific symposia and meetings
- A stimulating job in a dynamic multicultural team
- Swiss salary with generous social benefits
- 6 weeks holiday
If you are interested in a challenging position and working in the heart of Switzerland, please send your CV by e-mail to
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If you require further information, please call
Dr. Ian Leighton on +41 41 377 53 41 |
Placed 24/09/08 | |  | Miltenyi Biotec is an internationally operating biotechnology company based in Bergisch Gladbach near Cologne, Germany. The company was founded in 1989 and has rapidly expanded to become one of Germany’s largest biotechnology companies, now employing more than 1,100 staff. The product portfolio comprises reagents, instruments, and services for bioscience research and clinical applications, with a particular emphasis on cell separation, immunotherapy, and tissue regeneration. An exciting opportunity has arisen for | | Communication Managers (m/f) | | | to strengthen our Marketing Communications department. Reporting directly to the Head of Marketing Communications, this role requires the talents of an organized individual who is a self-starter and who will appreciate the scope of potential career development offered by Miltenyi Biotec and its global business. As part of the communications team, the Communications Manager will primarily coordinate the production of promotional material and copyedit a wide range of written work including customer journals, the internal company newspaper, advertisements, product catalogs, and product flyers. Working in close cooperation with the R&D department and product managers, he/she will generate and update product data sheets as well as hardware and application manuals. In performing these tasks, he/she will have an opportunity to specialize in subject areas that include instrumentation, molecular biology, stem cell biology and clinical cell therapies. The successful candidate should have a strong background in life sciences, preferably in cell biology, molecular biology, biophysics, hematology or oncology, and a proven track record of scientific communication. Copyediting experience is an advantage, and because the company language is American English, native English speakers will be preferred. The applicant should enjoy the challenge of communicating science to various target groups, that is, from scientific or clinical specialists to mainstream audiences. It is essential that the candidate has excellent project management skills and is able to organize and prioritize multiple projects. You will have the opportunity to work with highly motivated colleagues on advanced technologies in a dynamic, expanding biotechnology company. If you consider yourself a team player and feel ready for this challenge, please send us your resume to the following address. | | Miltenyi Biotec GmbH, Human Resources, Friedrich-Ebert-Str. 68, 51429 Bergisch Gladbach
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www.miltenyibiotec.com |
Placed 11/09/08  | Do you want more from your medical writing career? At PAREXEL, our Medical Writing team use their writing skills for more than just writing clinical study reports. We work on varied document types including patient information and informed consent forms, protocols, pharmacovigilance documents such as PSURs and ASRs, and regulatory submission documents such as clinical overviews. We are looking for a Senior Medical Writer to join our team. You will work with medical, regulatory and statistical staff as part of the clinical team, as well as providing medical writing expertise directly to our clients. You will join a small friendly group of writers, with all the opportunities and benefits offered by a large company such as PAREXEL. Within the group, there are excellent opportunities for career development. Our well developed training programme allows you to capitalise on the teaching provided by senior managers; several of whom are well known trainers within the medical writing industry. Candidates should ideally have experience in regulatory writing, and knowledge of preparing documents to ICH standards as well as proven organisational abilities, and excellent written and oral communication skills. All candidates must be fluent in written and spoken English. PAREXEL offers a competitive salary, including pension scheme, and a flexible working environment. The position is based in Uxbridge, UK. To apply please send your cv with a covering e-mail to:
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For further details on PAREXEL, and a detailed job description, please visit our web site at www.parexelcareers.com |  | 
Placed 28/08/08 | PRISM IDEAS Positions available: South Cheshire Medical Marketing Consultancy seeks leading Medical Writers with initiative Location: Nantwich, Cheshire Salary: Competitive remuneration package available Who we are: A dynamic and expanding Medical Consultancy and Communications agency with a broad client base. We operate a non-hierarchical editorial team and offer excellent future career prospects in an informal, friendly working environment. The role: Want to cut out the middle-man? We are looking for high calibre Senior/Principal Medical Writers who have the flexibility to write on a range of projects, fulfilling a multi-functional role by leading their own accounts and interacting directly with our clients. The individual: The successful candidate should have 1–6 years’ agency experience of producing high quality medical communications. He or she will posses excellent written/oral communication skills, while being organised, flexible and a good team player. Attention to detail is essential. To apply: Send a CV and covering letter to Diane Barber, Prism Ideas Ltd, Regent House, Princes Court, Beam Heath Way, Nantwich, Cheshire, CW5 6PQ Or electronically to
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(www.prismideas.com) |
Placed 21/08/08 |  Exciting medical writing role in Cambridge Medical Writer Napp Pharmaceuticals Ltd Napp Pharmaceuticals are looking for a Medical Writer to join our small friendly Medical Communications team on a short-term contract for approximately 9 months, although this could be longer. Your main role will be to work on a wide range of medical communications materials including marketing promotional and training materials. Ideally, you will have relevant experience in a medical communications agency or similar. This should include competence in managing multiple projects to meet deadlines and experience of working closely with internal customers at every stage of the process and building good working relationships. Educated to at least first degree level in a medically-relevant life science, you will need to demonstrate a flair for translating complex scientific information into plain English, a scrupulous attention to detail, the ability to learn about new therapeutic areas rapidly, and a passion for creating effective communications that target your audience. Benefits include a competitive salary, discretionary bonus, private medical scheme and pension scheme. To apply, please send your CV and a covering letter stating why you are interested in this contract, including details of your current salary package and notice period, to:
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For further information about the role, please email Kathleen Rosewarne, Head of Medical Communications and Education, on
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Closing date: Monday 8 September 2008 |
Placed 8/08/08 |  This leading International medical communication agency has been successfully delivering global communications strategies for almost 30 years. They deliver high standard marketing solutions to global pharmaceutical clients with dedicated client service teams based in London and New York. They are continuing to grow in size, enhancing the wealth of expertise now offering opportunities for enthusuiatic individuals. Senior Medical Writer – West London & New York Responsibilities will include: - Providing high‐quality writing and editorial services on a range of client projects
- Managing individual writing projects
- Coach and mentor less experienced writers in the team
- Liaise with clients and attend client meetings as required
- Acquire knowledge of therapeutic areas as required
In Return you will receive: - Excellent salary & benefits
- Be apart of a professional, friendly team
- Career progression & support
You must have a proven track record within a medical/healthcare communications agency. Opportunities are also available for their New York office. Please send your CV to
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for an immediate response. For all other vacancies within medical communications please contact me on +44 (0)1273 727930 |
Placed 8/08/08 | |  | | | | is a communication agency focussing on the health care business and located in Switzerland. We work primarily with international headquarters in Europe and the US, building consistent communication programmes from early product development right through to launch and beyond. Are YOU the medical writer we are looking for?
You will write a variety of scientific and regulatory documents on different topics. This involves the analysis of the raw data and a search of the literature.
Together with the project manager you will be responsible for the accuracy of scientific documents and ensure that deadlines and budgets are adhered to.
You will join the team for brain storming when solving the clients problems.
Although not directly involved in the project management you should have sufficient competence to support your project manager in dealing with the clients, opinion leaders and other involved parties. What can you offer us? - At least 2 years working experience in medical writing / medical communication
- Native English speaker
- A scientific background linked to medical science, preferably to PhD level
- Knowledge in a variety of therapeutic areas possibly including CNS, CVS or oncology
- Computer skills
- The ability to get along with different personalities
- Sound organizational skills
- Willingness to relocate to Switzerland. (Basic German would be a plus)
What can we offer you? - Challenging tasks in various projects running in parallel (early to late phase development of products)
- Involvement with the leaders of the pharmaceutical and medical device world
- Daily opportunities to learn something new
- Communication with multilingual counterparts from different cultural backgrounds
- The working spirit of an experienced professional group of people
- An environment where YOU make things happen!
- According to your abilities and expertise you can model your tasks / job description and define your personal development
- The fun and ambiente of working within an international team
Applications from qualified, motivated and positive-thinking individuals are welcomed.
Please send your résumé to:
archimed medical communication ag
Human Resources
Luzernerstrasse 30
CH-4800 Zofingen
Switzerland or to
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| |
Placed 7/08/08  |  | | | QIAGEN is one of the world’s most successful biotech companies and has achieved outstanding growth in its industry. As a worldwide leading provider of innovative DNA, RNA, and protein purification technologies, and molecular testing solutions to the life science market and to diagnostic laboratories, we have consistently delivered impressive year-on-year revenue increases. For our Global Marketing Communications Team in Hilden, Germany, we are currently seeking a: Senior Scientific Marketing Writer (f/m) | | | | |
Your responsibilities will be: - Writing compelling copy for marketing and corporate literature
- Contributing actively to the concept, structure, and contents of corporate literature and online projects
- Project management during concept, text, and layout phases
- Communication with internal and external partners
- Playing an active role in the Global MarkCom Team to implement corporate marketing strategies
| |
Qualifications required: - Native English speaker
- Molecular biology or similar background
- Ability to work in a team environment
- Excellent written and verbal communication skills
- Writing experience (e.g., PR, scientific, marketing, technical, medical, or other)
| | | |
If working in this challenging interdisciplinary area appeals to you, you will find a highly motivated team at QIAGEN looking forward to your support! Please send a full application, quoting the reference number MH-JP-SMW-08-EM, to the address below, or to
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. QIAGEN GmbH
Human Resources QIAGEN Strasse 1 40724 Hilden Germany www.qiagen.com | |  |
Placed 7/08/08 |  Medical writing opportunities - Hitchin, Hertfordshire
Choice Pharma is an expanding, dynamic company that supports biotech and pharmaceutical companies at every stage of the product lifecycle, from first-into-human studies to product launch and beyond. We provide the right blend of medical and scientific rigour, marketing expertise and impact communications to ensure that our clients achieve their business goals.
We are currently seeking experienced medical writers to join our growing team. Suitable applicants are likely to be graduates with a strong background in biomedical science (higher degree preferred), sound knowledge of one or more therapeutic areas, and experience of a range of medical writing projects, including developing manuscripts, posters, abstracts, publication plans, symposia, advisory boards, and educational programmes. Candidates will be extremely motivated, hard working individuals who take pride in delivering work of a high standard and have strong interpersonal and communication skills.
Choice Pharma can provide exceptional career development and personal growth opportunities by offering the opportunity to work on a wide variety of different projects and programmes for our clients. We offer an excellent salary and benefits package, and flexible working arrangements may be considered for outstanding candidates. If you are seeking a fresh approach to your medical writing career, please forward your CV to
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, outlining your salary expectations and enclosing two recent examples of your work. |
Placed 7/08/08 |  Excerpta Medica, an Elsevier business, is a leading medical communications agency that partners with the pharmaceutical industry to educate the global healthcare community. At Excerpta Medica, we think, create, and deliver a full line of strategic solutions in the areas of Strategic Publication Planning, Medical Communications, Medical Education, Medical Publishing, and Interactive Solutions. As a result of a significant increase in business, we are looking to appoint talented, experienced Publication Managers (London or Amsterdam based)
Strategic Publication Planning Our Publication Managers are not only responsible for preparing high-quality, medically accurate documents, but also for developing and driving strategic publication plans, client management, and identifying opportunities for new business. Successful candidates will have: - Drive and ambition to succeed
- Experience in strategic publication planning and client liaison
- PhD in life sciences (or relevant work experience plus a lower-level bioscience degree)
- Proven experience in a medical communications agency or pharmaceutical company
- Excellent command of the English language and outstanding writing and communication skills
- Exceptional attention to detail.
With offices in the vibrant cities of Amsterdam and London, Excerpta Medica will offer you the opportunity to broaden your horizons by working in an international and multicultural dynamic organization, structured monthly training programs, and the development of your scientific, marketing and communication skills, with well-educated and dedicated colleagues. Remuneration packages are highly competitive and commensurate with experience. Valid EU work permit required. For further information or to apply, please send a cover letter and curriculum vitae to Wilma Verhoef on +31 (0)20 485 3975 or at
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quoting job reference EMPMEMWA01 |
Placed 18/07/08 | | | | QIAGEN is one of the world’s most successful biotech companies and has achieved outstanding growth in its industry. As a worldwide leading provider of innovative DNA, RNA, and protein purification technologies, and molecular testing solutions to the life science market and to diagnostic laboratories, we have consistently delivered impressive year-on-year revenue increases. For our Global Product Management Team we are currently seeking a: Technical & Marketing Writer (m/f) for our office in Hilden (near Düsseldorf), Germany or Crawley, UK | | | | |
Your responsibilities will be: - Writing effective technical and compelling marketing literature
- Contributing actively to content of literature and online projects
- Coordinating preparation of materials during text and layout phases
- Communication with internal and external partners
- Playing an active role in the Global Product Management to implement corporate marketing strategies
| |
Qualifications required: - Native English speaker
- Molecular biology or similar experience
- Ability to work in a team environment
- Excellent written and verbal communication skills
- Ideally first writing experience
| | | |
If working in this challenging interdisciplinary area appeals to you, you will find a highly motivated team at QIAGEN looking forward to your support! Please send your application, quoting the reference number MH-KS-TMW-06, to the address below or to
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. QIAGEN GmbH Human Resources QIAGEN Strasse 1 40724 Hilden Germany www.qiagen.com | | |
Placed 17/07/08  | | Celgene (www.celgene.com) is a global biopharmaceutical company focused on the discovery, development and commercialization of innovative therapies for unmet medical needs in cancer and inflammatory diseases. Celgene employs over 2000 people worldwide and is quoted on the NASDAQ stock exchange. As a recent key milestone, Celgene has established its International Headquarters and global production site in Neuchâtel, Switzerland. In order to further strengthen our team and to manage our rapid growth and very promising product pipeline, we are currently looking for our new : | | | | | Manager Medical & Scientific Writing Reporting to the Associate Director, Medical & Scientific Writing Europe and working in a small team, responsibilities will include the following: - Working with other relevant line functions, prepare phase 1 – IV clinical and regulatory documents and submissions, including Investigator Brochures, clinical study reports, integrated summaries of efficacy and safety, registration dossiers, package inserts, and responses to health authorities.
- Participate in study and clinical team meetings and assist the teams in resolving issues related to document preparation.
- Review data to determine the appropriate tabular and textual formats, and the clarity, logic and order of presentation.
- Prepare internal guidelines for document preparation.
- Prepare templates for clinical documents that are consistent with FDA and ICH guidelines and with electronic submission guidelines.
- Develop the strategy for document preparation, including time frames that meet or exceed company standards and the document review processes.
- Facilitate document review meetings and discussions.
- Participate in the development of outsourcing plans for medical writing
- Manage outsourced medical writing projects
- Review work of other writers (in-house or contract) for accuracy, quality, focus, and adherence to format and stylistic requirements.
- Train and guide other writers (in-house or contract) in company policies and procedures related to document preparation.
- Assist with preparation of presentations for major external meetings.
- Assist with transferring and presenting clinical / regulatory data to Marketing for journal submissions
Skills/Knowledge Required: - BS/BA degree in Biomedical Science (Masters preferred)
- 5+ years in the pharmaceutical industry or in a CRO, including 3+ years’ writing experience
- Extensive experience writing all types of clinical & regulatory documents and with registration dossiers for worldwide use
- Knowledgeable in preclinical development including discovery, toxicology etc.
- Knowledge of FDA and ICH guidelines
- Knowledgeable in industry trends for study reports and international dossier preparation, including electronic document submissions (eCTD)
- Ability to work with complex projects and within cross-functional teams
- Experience working with CROs
- Expertise in multiple therapeutic areas
- Fluent English - excellent grammatical and communication skills, both written and oral
Your prospects:
A unique opportunity to join one of the world’s most successful biopharmaceutical companies with a great future. The chance to actively participate in the setting-up of the International HQ with a broad range of responsibilities in a very dynamic and motivating environment. Real personal and professional development opportunities coupled with an attractive compensation package. If you are interested in joining our team, submit your CV by email to:
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|
Placed 11/07/08 |  RSA is a leading European provider of resourcing services to the Life Science and Healthcare sectors. The company consists of 7 offices in France, Germany, Switzerland, Singapore, USA and the headquarters in the United Kingdom (2 offices: Hatfield and London). For one of our client, we are looking for: Position: Medical Writer Location: Vienna, Austria Our client is one of the leading suppliers of biopharmaceuticals for the prevention and treatment of many life-threatening conditions. These life saving products treat or protect against many conditions such as haemophilia, immune deficiency disorders, Rhesus factor complications in pregnancy, infectious disease and tissue sealing for surgical patients. Position Description: - Write and review documents pertaining to clinical research and medical affairs
- Write clinical study reports, protocols, interim reports, annual reports, investigator’s brochures and scientific publications
- Assist in submission of documents to regulatory agencies and medical/scientific journals
- Keep up to date with current developments in regulations and perform trainings for clinical staff in this context
Requirements: - Scientific background + 3 years of experience in Medical Writing is preferred or Non-scientific background + 5 years of experience.
- Excellent command of oral and written English (near-native preferred)
- Previous experience in clinical drug development or scientific editing an advantage
For further information, please send a CV and cover email to the following with Ref. Nr: 08636. | RSA Consulting GmbH
Stuttgarter strasse 25-29
D-60329 Frankfurt am Main Stéphanie Rivière
Project Manager
Tel: +49 69 219 776 0
E-mail:
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| www.theRSAgroup.com
www.rsajobs.com | | Hatfield ■ London ■ Frankfurt ■ Baar ■ Paris ■ Singapore ■ Morristown | |
Placed 7/07/08 |  Safety Medical Writer
International Product Safety (IPS) has 2 vacant positions as Safety Medical Writer in our recently established Safety Medical Writing Group located in Copenhagen (Denmark). The Safety Medical Writing Group is a new, very dynamic team with success and fun as important words in our daily work! As there is an increasing focus on drug safety, we continuously strive to improve our processes and educate/train ourselves to ensure we can act as expert collaborators Challenges:
IPS has the global responsibility for Pharmacovigilance at Novo Nordisk (NN). The Safety Medical Writing Group is responsible for writing the major external safety regulatory reports in IPS. As a safety medical writer you will act as project manager for planning, coordinating and writing our key safety documents: Periodic Safety Update Reports, Risk Management Plans, and Annual Safety Reports for all NN marketed products and clinical development projects. The role involves data analysis and writing complex documents at a professional level in close collaboration with people from different departments and with different professional and cultural backgrounds. All documents are written in English, and must comply with NN standard operating procedures and external guidelines. Participation in the ongoing standardisation and improvement of processes is also an important component of the job. Further you will be involved in the development of the new group! Qualifications: You have a university degree in a biomedical discipline (MD, PhD, MSc or equivalent) and experience with medical terminology, analysis and presentation of data. Excellent written and spoken English and a flair for and interest in scientific communication are expected. You have experience with writing scientific reports and/or publications for scientific journals. High level experience with MS Word, Excel, PowerPoint and internet facilities is a must. You are organised, systematic, pay attention to detail and quality, and are able to work well under pressure and meet tight deadlines. You are a team player, good at establishing contact with partners and have a good sense of humour.
.
Contact: For further information please contact Jenny Kastberg +45 3079 4470 or Pilar Carrero +45 3075 7476 Please forward your application online at novonordisk.com marked “NN41489 Safety Medical Writer”.  |
Placed 02/07/08
|  Medical Writing Manager - Oncology Stockley Park - West London, England Collegeville, Pennsylvania This highly visible, leadership role will include direct responsibility for strategic development, planning, writing, and management of clinical documents associated with the life cycle of (an) Oncology key asset(s). Including, Phase I-IV clinical study reports, Investigator's Brochures, CTD clinical overview and summaries of safety and efficacy, briefing documents, regulatory responses, clinical sections of IMPD for clinical trial application and required regulatory annual reports.
Key responsibilities: - Successfully lead the matrix team in clinical document planning and development.
- Key contributor to Oncology MDC clinical strategy, demonstrating in-depth knowledge and understanding of regulatory requirements including Good Clinical Practice (GCP) and other regulations governing clinical research, ICH guidelines for Common Technical Document (CTD) and Code of Federal Regulations (CFR) for New Drug Application and FDA requirements.
- Self-starter with proven ability to quickly assess complex situations, apply scientific, operational and submission development experience to identify and implement effective solutions as to conflicts.
- Independently plan submissions, recommending innovative solutions for achieving accelerated timelines, demonstrating an understanding the interdependencies of various contributing functions
Qualifications Required: - Graduate in a scientific discipline.
- In-depth understanding of clinical research principles and global registration requirements for pharmaceutical compounds.
- Have a proven track record of success in leading a matrix team in the development of strategies and preparation of major clinical dossiers or major country regulation submissions.
- Qualified candidates with a keen interest in Medical Writing who are currently within Regulatory Affairs or Clinical Research will be considered for this opportunity.
Please note:Preference will be given to applications received by Monday 21st July. To Apply: Please apply online by clicking the button below:  All data processed in accordance with the provisions of the Data Protection Act. GSK is an equal opportunities employer and is proud to promote an open culture. To enable GSK to meet its commitment as a two ticks employer please let us know if you have a disability. |
Placed 02/07/08 | Do you want more from your medical writing career? At PAREXEL, our Medical Writing team use their writing skills for more than just writing clinical study reports. We work on varied document types including patient information and informed consent forms, protocols, pharmacovigilance documents such as PSURs and ASRs, and regulatory submission documents such as clinical overviews. We are looking for a Medical Writer to join our team. You will work with medical, regulatory and statistical staff as part of the clinical team, as well as providing medical writing expertise directly to our clients. You will join a small friendly group of writers, with all the opportunities and benefits offered by a large company such as PAREXEL. Within the group, there are excellent opportunities for career development. Our well developed training programme allows you to capitalise on the teaching provided by senior managers; several of whom are well known trainers within the medical writing industry. Candidates should ideally have experience in regulatory writing, and knowledge of preparing documents to ICH standards as well as proven organisational abilities, and excellent written and oral communication skills. All candidates must be fluent in written and spoken English. PAREXEL offers a competitive salary, including pension scheme, and a flexible working environment. The position is based in Uxbridge, UK. To apply please send your cv with a covering e-mail to:
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For further details on PAREXEL, and a detailed job description, please visit our web site at www.parexelcareers.com | |
Placed 25/06/08 | | | After 7 years of significant growth, Fishawack is now one of the largest independent specialist communications agencies in the UK. It is the mix of individuals united by a single philosophy that underpins the ‘Fishawack difference’ of excellence, creativity and fun. We are looking for talented individuals to join our editorial teams in Knutsford, Cheshire and Abingdon, Oxfordshire. Medical Writer
Do you have strong written and verbal communication skills and a keen eye for detail? Are you either a life science graduate with previous medical writing experience or a life science postgraduate ready for a new opportunity? We are looking for enthusiastic writers to join our editorial team in delivering high-quality promotional and educational projects for our pharmaceutical clients. If you believe you can make a positive contribution to our team, please submit your CV to Sara Henshall, Fishawack Communications Ltd, 100-102 King Street, Knutsford, Cheshire. WA16 6HQ, email (
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), or via our website (www.fishawack.com).  | | | |
Placed 25/06/08 | | | Two roles - A highly motivated and professional Senior Medical Writer, or promotion-ready Medical Writer (2 yrs+ experience)
- Managing Editor/ Director, Medical Education (4/5 yrs + experience).
About us A small, friendly healthcare communications agency in London’s Docklands; these are exciting opportunities to realise your potential and contribute to the direction and growth of a young agency, within a passionate and expanding high-calibre team. About you Whichever role is you, you have a PhD (/life sciences degree), and a passion for the written word in med comms. Able to use language to influence and engage a variety of audiences, you are comfortable writing scientifically, promotionally or strategically, and have the detail focus to ensure highest QC standards. You are attuned to the demands of pharmaceutical communications, have the commercial aptitude to integrate with the agency’s business development activities and the desire to make your mark. Managing Editor/ Director, Medical Education. You are sharp, hard-working and ambitious editorial professional with international med comms experience and an entrepreneurial streak. As you contribute to business growth, you will grow your own editorial department. Meanwhile, you are happy to muck in with editorial content development, and very comfortable with strategy and business development. Skills - Flawless grammar, excellent science writing and a non-scientific editorial flair
- Basic analytic capabilities and comfort dealing with data
- Proven time-management and prioritisation across multiple projects
- Strong work ethic, high standards and integrity
- Microsoft Office, essential: a passion for e-media, helpful
- Eye for detail
- Relevant agency experience required
- Proven ability to keep sense of humour under pressure
- CNS / addictions experience advantageous.
Managing Editor/ Director, Medical Education: Additional Skills - Supportive and collegiate management style
- Proven track record in contributing to business development and running happy and effective editorial teams
Training
Structured development and tailored training opportunities will help the right candidate to progress quickly in a fast-moving, exciting working environment.
Please apply to
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, indicating salary expectations.
| | | | |
Placed 2/06/08 | This global healthcare communications agency has a track record of consistent growth. They have over 20 years' experience of developing and implementing medical communications programmes around the world. Their success in the global pharmaceutical environment is based on and continues to be driven by their staff. Working together as dedicated client teams, they provide specialist skills to maintain the high standards for which they have become internationally recognised. Editorial Team Leader - Cheshire
You will: *manage internal writers’ and editors’* ensure provision of appropriate editorial resource for projects and accounts * have extensive skills in writing editing and editorial management * act as editorial lead for client accounts Senior Medical Writer – Cheshire/Home Based
You will: *be writing on a senior level * review the work, mentor and develop junior medical writers * proactively develop new business for existing and new clients * establish/develop and maintain opinion leader relationships
In return you will recieve: *excellent salary *car allowance *25 days holiday *pension *Support & Training for career progression Please send your CV to
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for an immediate response. For all other vacancies within medical communications please contact me on +44 (0)1273 727930 |
Placed 30/05/08 | A revolutionary new clinical decision support publication.
Your break into clinical editing. Clinical Editors
12-month contracts or 6 month (working 5 days per week)
Competitive salaries * London This is an exceptional chance for six doctors or pharmacists to move out of practice for a year or possibly longer, joining us as Clinical Editors on a new BMJ clinical decision support publication. You will be creating and editing authoritative content for BMJ Best Practice – an international website providing a comprehensive guide to diagnosis and treatment of a broad range of clinical conditions. The roles involve editing original commissioned material, assessing the quality of clinical guidance, and creating formats for different global markets. The positions also involve working with national and international expert authors, global opinion leaders, and strategic partners. You may also occasionally represent the product in the public arena. You should have experience of editing or writing for medical publications and a practical understanding of evidence-based medicine, along with an innovative, creative and flexible approach to information delivery. It goes without saying that you will be able to communicate complex concepts to a range of audiences in a clear and effective way, both written and verbally. You will also need the ability to learn quickly, work to tight deadlines, and contribute to a highly talented team.
For more information on the role or the BMJ Group, please visit www.bmjgroup.com or to discuss the roles further, please email Mark Stuart, BMJ Best Practice Deputy Editor at
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This is an exciting time for evidence-based healthcare and electronic medical information. If you’re keen to bring your clinical experience to an internationally recognised leader in this field, please send your CV, covering letter and salary details to: HR Team, BMJ Group, BMA House, Tavistock Square, London WC1H 9JR, or email
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Closing date: Monday 23rd June 2008. |
Placed 30/05/08 | | | | Boehringer Ingelheim ranks among the world's 20 leading pharmaceutical corporations. Our vision drives us forward. It helps us to foster value creation through innovation in our company and to look to the future with constantly renewed commitment and ambition. | | | At its site in Ingelheim, Boehringer Ingelheim Pharma GmbH & Co. KG produces medicines and drug substances for the international corporation and is responsible for marketing and sales within Germany. | | | | | | | | | | | | We now seek to recruit the Head of Safety Writing m/f to lead our new safety writing team in Ingelheim, Germany. This is an excellent opportunity to be at the heart of Drug Safety – taking responsibility for key safety documents. | | As part of the Drug Safety Regional Center Europe of Boehringer Ingelheim, your role will be to plan and to write key safety documents such as Periodic Safety Update Reports, ensuring that they meet the highest standards of quality, accuracy and organisation. You will be heading a team of writers, working closely with drug safety, medical and regulatory colleagues to plan content, review and interpret data, draft documents, accommodate feedback and ensure that all aspects of documentation are adequately planned and executed. | | Together with an MD, PhD, MSc or equivalent in a biomedical discipline, you will need to have previous writing experience and to demonstrate a clear, concise scientific writing style. Excellent command of the English language and medical terminology are indispensable for success in this position. Equally important will be your leadership skills, flexible approach, attention to detail, and the ability to work on a variety of projects and documents within schedule across different therapeutic areas. Previous experience in a pharmaceutical company would be a major asset, particularly if this included involvement in the preparation of safety documents like Periodic Safety Update Reports. This is a globally focused, highly challenging role, where you will take responsibility for your team and projects. The position calls for a accurate, persuasive, influential and decisive approach, with a talent for cross-culture communication. In return Boehringer Ingelheim offers stimulating career development with a suitable remuneration and benefits package. You will be based in Ingelheim near Frankfurt, Germany, working in a multi-disciplinary, international and dynamic environment. | | | | For further information please contact: Dr. Rainer Heißing,
+ 49 (0) 61 32 / 77 42 57. | | | If you are seeking opportunities to expand your professional horizon and your profile corresponds to the above, we look forward to hearing from you. | | | Boehringer Ingelheim
Pharma GmbH & Co. KG
A Personalmanagement
Astrid Hanß
55216 Ingelheim am Rhein
Germany
Phone:
+49 (0) 61 32 / 77 95 129 | | | | | |
Placed 30/05/08 |  nspm ag
is a successful medical communications company located in Switzerland. We implement clinical and marketing projects for international customers in the pharmaceutical industry. nspm provides a complete medical writing service across a broad spectrum of therapeutic areas, with the experience and expertise of our highly qualified in-house medical writers. For our team we are currently looking for a MEDICAL WRITER / PROJECT MANAGER YOUR PROFILE - University degree and higher education (PhD/MD) in medicine, natural or health sciences, or pharmacy
- English mother tongue
- Editorial or medical writing experience in the pharmaceutical industry is desirable
- Computer literacy (PowerPoint/Word)
YOUR MAIN RESPONSIBILITIES - Writing and editing medical texts, including abstracts, publications and slides
- Proofreading texts
- Organising scientific symposia and meetings
- A stimulating job in a dynamic multicultural team
- Swiss salary with generous social benefits
- 6 weeks holiday
We offer a stimulating job in a dynamic team environment. If you are interested in a challenging position in the heart of Switzerland, please send your CV by e-mail to
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If you require further information, please call
Dr. Ian Leighton on +41 41 377 53 41 | | 
Placed 29/05/08 |  Novartis is a world leader in offering medicines to protect health, cure diseases and improve well-being. The organisation consists of four different business divisions; Novartis Vaccines is one of them. They provide innovative vaccines and a wide range of conventional products to eliminate viral and bacterial diseases across the globe. Portfolio of products includes vaccines for influenza, meningitis, rabies, polio, measles, rubella, diphtheria and tetanus. For our office in Amsterdam we are looking for two PUBLICATION MANAGERS JOB PURPOSE
Participating in the creation of Publication Strategies and ensuring the implementation of the resulting Publication Plans for Novartis Vaccines products to ensure scientific support of marketing objectives and company compliance with data disclosure legislation. MAJOR ACCOUNTABILITIES - Management of Publication Plans to meet requirements of company Publication Strategies.
- Write publications from clinical and epidemiological studies reports, and health economic analyses (abstracts, presentation, posters and peer-reviewed manuscripts) – becoming the referent for these types of articles
- Coordinate the internal & external review of manuscripts,
- Submit validated manuscripts to biomedical journals,
- Follow-up the process to ensure timely publication,
- Guarantee compliance of publication activities with internationally accepted ethical standards and the company's quality standards,
- Participate in specific publication committees.
EDUCATION / EXPERIENCE
Desirable degrees: PhD in life sciences
Languages: English mother tongue
Experience / professional requirements: - 2-3 years experience in communication and/or publication planning and implementation
- Attention to detail, and creative
- An excellent knowledge of medical & scientific publication methodologies
- A good knowledge of biomedical and scientific peer-review journals.
Are you searching for a new challenge and do you think you qualify for this position, then please go to our website www.novartis.com and apply. |
Placed 29/05/08  | Are you looking for an exciting new challenge and the right opportunity? Join the Envision Pharma team – we have clients across the globe and offices in the UK and USA. With a range of unique scientific and cuttingedge technology solutions including Datavision, we are market leaders in medical communications. Due to significant expansion we have opportunities for medical writers and scientific team leads which offer exciting challenges in a scientifically stimulating environment. Ideally, you will have worked in medical communications and have a relevant higher degree (or equivalent). A proven track record of medical writing and editing, plus an exceptional eye for detail are essential. As a medical writer/scientific team lead you will (depending on level of experience) demonstrate excellent writing and quality control, serve as key client/author liaison, champion key therapeutic areas, be responsible for managing your projects and successfully delivering outputs, instruct/ mentor other medical writers, and have an appreciation of the nuances of publication planning, strategy and implementation. Yes, you will be conversant with the many and varied tasks of a scientific, medical communication professional. We are a dynamic and rewarding company to work for, with excellent benefits and an informal, friendly, and vibrant work environment. Please email your CV to
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or alternatively visit www.envisionpharma.com for the latest career opportunities.
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Placed 15/05/08 |  At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance's impressive history of company stability and growth. We've achieved these results by fostering a work environment that encourages, develops and leverages our team's capabilities. Covance's ongoing success offers team members unsurpassed growth and career development opportunities. There is no better time to join us! Senior Medical Writer At our central Leeds site, we are currently recruiting for a Senior Medical Writer, to join a department comprising 7 Medical Writers and 2 Editorial Assistants . The successful candidate will act as a scientific leader of the Pharmacometrics' project team on the conduct and reporting of Phase I/II studies. They will provide guidance and leadership to ensure successful project completion. Key duties will include the preparation of draft and final clinical study reports (CSRs) for Covance CRU and contract Phase I/II studies, along with the production of scientific publications and other documents (e.g. protocols, abstracts etc) to sponsor requirements. You will also author scientific papers, which are published in peer-reviewed journals and provide and develop intra-and inter-departmental training. Finally, the candidate will be responsible for the provision of training and mentoring of Associate Medical Writers and Editorial Assistants along with scientific presentations both internally within Covance CRU and externally (e.g. conferences). You will Typically have 3 - 4 years' medical writing experience with a BSc Life Sciences degree or higher At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. Apply Online: www.covancecareers.com  | |
Placed 7/05/08 | Actelion Ltd is a biopharmaceutical company with its corporate headquarters in Allschwil/Basel, Switzerland. Its first drug Tracleer® has been approved as a therapy for pulmonary arterial hypertension and is marketed through subsidiaries in key markets worldwide. As a leading player in innovative science related to the endothelium, which separates every blood vessel from the blood stream, Actelion focuses on the discovery, development and marketing of innovative drugs for significant unmet medical needs. Actelion shares are traded on the SWX Swiss Exchange (ticker symbol: ATLN). In our Clinical Development department we are seeking a Senior Medical Writer to establish and lead an in-house medical writing group, and to manage external medical writing services. You will be responsible for writing and reviewing clinical regulatory documents such as clinical study reports, investigator’s brochures, and CTD Module II summaries, in collaboration with Regulatory Project Managers, Clinical Science Leaders, and the International Project Team. You will also assist in the preparation and review of clinical study protocols and statistical analysis plans. You will work together with the in-house Documentation Group to coordinate documentation services for Clinical Development and produce high-quality documents in compliance with regulatory requirements. The ideal candidate should have: - A degree in life sciences or medicine (PhD or MD)
- English mother tongue
- Highly developed and proven medical writing skills
- At least 5 years of experience as a medical writer in the pharmaceutical industry across several therapeutic areas
- The ability to mentor and develop junior medical writers
- Line management experience
- Knowledge of regulatory document requirements and guidelines
- The ability to work independently and as part of a team
- The ability to work under pressure and meet challenging deadlines
- Excellent interpersonal and presentation skills
We offer: - A competitive salary and generous social coverages
- The possibility for development and advancement within a constantly growing company
- An innovative and stimulating atmosphere within a multicultural environment
The research facilities are located in Allschwil, Switzerland, a suburb of Basel on the borders of France and Germany. | | Please send a comprehensive application in English to: Human Resources
Attn: Michel Petignat
ACTELION Pharmaceuticals Ltd
Gewerbestrasse 16, 4123 Allschwil / Switzerland Electronic applications are welcome. Please refer to our Website: www.actelion.com/JobHQ | | |
Placed 7/05/08 |  Kelly Scientific Resources® (KSR), a division of Kelly Services, is the world’s leading partner for scientific staffing. We provide competent knowledge of the pharmaceutical, chemical and biotechnological industry as well as experienced consultancy.
Our customer, Crucell, is headquartered in Leiden/NL, having approximately 1’100 employees worldwide. Crucell, Berna Biotech Ltd., sells oral vaccines against typhoid fever, travelers’ diarhea and innovative vaccines against influenza, hepatitis A, hepatitis B and other infectious diseases.
To join the Clinical Development Department of Crucell, Berna Biotech Ltd. in Berne/Switzerland, we are looking for an in-house Medical Writer
(m/f) 100 % Your Responsibilities:
You supply services and provide medical writing and scientific expertise to the clinical project teams. Writing and editing of clinical and regulatory documents as investigator brochures, clinical study protocols and reports will be your main responsibilities. In this context you manage the review process of clinical documents and ensure that timelines are met. For answering inquiries from regulatory authorities regarding clinical studies, you will assist in preparing responses. Further, you write, edit and design a wide range of communication material such as abstracts, congress posters, manuscripts for journals or summaries of clinical studies. Maintenance and updating of document templates as well as participation in process improvement will be self-evident for you. Your profile:
You hold a life sciences degree or an advanced degree in English with scientific education and training. Excellent written and oral communication skills, attention to detail and quality, service-oriented personality, organizational and time management skills are expected. Also the ability to work effectively both independently and in a team is assumed. You should have 2-3 years medical writing experience in a pharmaceutical company or CRO, be fluent in English (native speaker or stay abroad) and possess a high level of proficiency in MS Office, particularly in Word, generation of tables and graphics, PowerPoint presentations and templates. A flair for the interpretation of figures would be an additional asset. Interested candidates please mail CV and references to: Ruth Meinke, Kelly Scientific Resources, Barfüsserplatz 6, 4001 Basel/Switzerland, phone 0041 61 270 80 10,
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Placed 1/05/08 |  Senior Medical Writers
Location: Oxford and London Looking for a challenging and creative role within a leading Medical Education Agency? Ogilvy 4D and Ogilvy Healthworld Medical Education are both award-winning companies within Ogilvy Healthworld UK. Due to increasing growth they require Senior Medical Writers to join their busy teams in Oxford and London. The successful candidates will have excellent writing skills and a background in the Medical Communications or Pharmaceutical Industries would be useful. A life sciences degree is essential and a Ph.D or M.Sc desirable. As a Senior Medical Writer, you will have the skills to work with clients at a strategic level and convey key scientific messages to a broad audience concisely and effectively, and within the parameters of the client brief. You will ensure that work is of a high scientific and literary standard, have exceptional attention to detail, and have the ability to work creatively and accurately under pressure. Client liaison will also play a key part in this role, and the successful candidate will need an understanding of the role of Medical Education in the Client’s business environment. If you think you may have the skills and desire to succeed in this role, please send your CV, preferred location and salary expectations to
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Placed 30/04/08 |  Chief Medical Writer and Editorial Director – Medical Communications (London)
Competitive salary and benefits The Nucleus Group includes the medical communications agencies MediTech Media and Health Interactions, and the medical publisher International Medical Press. With over 350 employees in ten offices around the globe, we place the highest value on the scientific knowledge and expertise of our employees, which are key to the level of service we supply to our clients. We are currently seeking two Editorial Directors to head up editorial services: one for MediTech Media and one for Health Interactions. The successful candidate will lead and motivate a large team of Medical Writers, Senior Medical Writers and Chief Medical Writers who combine powerful writing skills with expertise in medical science to deliver engaging content for Nucleus’ products. You will be responsible for building on the Company’s established reputation for scientific integrity and writing excellence in medical education programmes by monitoring and improving the quality and content of the services provided to clients. You will be working with account handlers and editorial teams to develop innovative and cost-effective solutions to meet clients’ marketing and communication objectives and by providing strategic consultation to clients. We are also seeking a Chief Medical Writer with a strong background in virology. You will be responsible for managing a team of medical writers and for delivering a diverse range of high-quality scientific materials for our virology accounts which focus on HIV, HBV, HCV, CMV and influenza. You will be responsible for researching specialized areas of medical science in order to write and edit text as well as working with design and production teams to produce a range of printed and computer-based materials to meet the needs of Nucleus’ clients. The role may also involve interacting with outside scientists and physicians on critical therapeutic and scientific issues. To succeed in either role you will be qualified to PhD or MSc level, with a wealth of experience in a medical communications agency or pharmaceutical company. To find out more please go to www.nucleusholdings.org, or, to apply, please send a copy of your CV to
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Placed 25/04/08 |  Trilogy Writing & Consulting GmbH is a young, dynamic, growing company based in Frankfurt am Main, Germany that produces regulatory documentation and scientific publications for the international pharmaceutical industry. We currently have vacancies for: - Medical Writers
- Senior Medical Writers
Do you enjoy writing?
Do you have good interpersonal skills and work well in a hectic environment?
Can you stay focused under tight timelines? Then this may be the job for you. For the Medical Writer positions, no experience in medical sciences is required, but you must have the following: - Diplom/Magister or Bachelors degree in science (PhD not necessary)
- Fluent written and spoken English skills
- An appreciation for a well written document
- Enjoy proactively participating on a team with diverse personalities
- Flexibility
- An eye for details
In addition to the above, for the Senior Medical Writer positions, you will need to have at least 3 years experience actively writing regulatory documents. As a Medical Writer at Trilogy Writing we will teach you to provide a service to clients that offers more than just writing. Our writers are integral parts of clinical development teams with the world’s largest pharmaceutical companies. We assist those teams in writing and coordinating successful documentation across a broad spectrum of therapeutic areas, whether it be for regulatory submission packages or for publication in scientific journals. As a young company, there is room to grow and develop with us… and your ideas will form our future together. For further insight into who we are and what we do, please look at our website. Remuneration will be appropriate for the corresponding position, with all standard German benefits. If you are interested in exploring where your own creative input can take you, contact us. For further information about the positions, feel free to call Dr. Julia Forjanic Klapproth at 069 255 39511. To apply, please write in English with your CV to Dr. Julia Forjanic Klapproth, Trilogy Writing & Consulting GmbH, Falkensteiner Str. 77, 60322 Frankfurt am Main or
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Placed 24/04/08 |  We Innovate Healthcare. About Roche
Headquartered in Basel, Switzerland, Roche is one of the world’s leading research-focused healthcare groups in the fields of pharmaceuticals and diagnostics. As the world’s biggest biotech company and an innovator of products and services for the early detection, prevention, diagnosis and treatment of diseases, the Group contributes on a broad range of fronts to improving people’s health and quality of life. Roche is the world leader in in-vitro diagnostics and drugs for cancer and transplantation, and is a market leader in virology. It is also active in other major therapeutic areas such as autoimmune diseases, inflammatory and metabolic disorders and diseases of the central nervous system. We now seek to recruit an Experienced Medical Writer to join our team in Welwyn Garden City, UK. This is an excellent opportunity to be at the heart of the drug development and licensing process — taking responsibility for key documentation projects and driving them through to fruition. As part of the Pharmaceutical Development division of Roche, you'll also be working at the leading-edge of the pharmaceutical industry, helping to bring important new medicines to market. Your role will be to plan and to write key clinical regulatory documents (including clinical study reports, investigator brochures, clinical summaries and overviews), ensuring that they meet the highest standards of quality, accuracy and organisation. As a key member of global project teams you will be working closely with statistical, scientific and medical associates to plan data tabulations, review and interpret data, draft documents, accommodate feedback and ensure that all aspects of clinical NDA/MAA documentation are adequately planned and executed. Together with a PhD, MSc or equivalent in a biomedical discipline, you will need to have previous medical writing experience and to demonstrate a clear, concise scientific writing style. Equally important will be your flexible approach, attention to detail, and the ability to work on a variety of projects and documents within schedule across different therapeutic areas. Previous experience of clinical research and development in a pharmaceutical company would be a major asset, particularly if this included involvement in the preparation of high level clinical summaries and in regulatory filings.
It's a globally focused, highly challenging role, where you will take responsibility for your own project within a supportive, close-knit team. So, it calls for a detail-conscious, persuasive, influential and decisive approach, with a talent for cross-culture communication. In return Roche offers a competitive salary plus the excellent benefits you would expect from a blue-chip organisation, including a genuine interest in your development and progression, together with a modern, state-of-the-art office environment. To be considered for this position, please apply at http://careers.roche.com/uk. When completing your application, please ensure you attach an up to date CV and details of your current remuneration package. |
Placed 12/04/08 | PRISM IDEAS Positions available: South Cheshire Medical Marketing Consultancy seeks leading Regulatory Medical Writer with initiative Location: Nantwich, Cheshire Salary: Competitive remuneration package available Who we are: A dynamic and expanding Medical Consultancy and Communications agency with a broad client base. We operate a non-hierarchical editorial team and offer excellent future career prospects in an informal, friendly working environment. The role: We are looking for a high calibre Regulatory Medical Writer who has the flexibility to work on a range of projects over several therapy areas. The individual: The successful candidate should have 1–6 years’ agency experience of producing a range of high quality regulatory materials. He or she will posses excellent written/oral communication skills, while being organised, flexible and a good team player. Attention to detail is essential. To apply: Send a CV and covering letter to Dr Colin Hayward, Prism Ideas Ltd, Regent House, Princes Court, Beam Heath Way, Nantwich, Cheshire, CW5 6PQ
Or, electronically to
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(www.prismideas.com) |
Placed 3/04/08 | FREELANCER NEEDED An established medical publishing firm functioning as the publishing arm of a larger medical education/communications company has is an opportunity for an experienced medical writer to attend assigned sessions at the European Congress of Microbiology and Infectious Diseases (ECCMID) in Barcelona Spain between April 19-22……..Will capture key content and write three -four articles totaling app. 3,000 words (range between 300 and 1,000 words per article) for a medical newspaper, Conference Perspectives. Specific direction and guidance will be provided in advance, including specific objectives of each article……Must be experienced in medical news reporting (different from peer-reviewed journal writing) and be familiar with current AMA writing style…….Writers will be responsible for submitting all completed manuscripts electronically, within three days (72 hours) of the official completion of the conference……. Must also send by overnight courier all support materials (official conference program, presentation slide decks, presentation hand outs, “permissions to use”, audio tapes, reference materials, hard copies of each written manuscript, suggested figures and tables, annotated meeting materials) to also arrive to Dothen editor no later than 72 hours following official completion of the conference.…….Writers will be compensated at the rate of $1.00 (US) per word plus $100 (US) per diem for each day attending sessions. Partial relief for travel expenses will be considered……. Interested parties should respond to
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with attached resume, writing samples (especially on infectious diseases), and your thoughts on why you think you’ll be a good fit for this assignment. Martin Zittel President/Publisher
Dothen Healhtcare Press
A Strategic HealthCOM Company
25 Lindsley Drive, Suite 208
Morristown, NJ 07960
USA |
Placed 24/04/08 | We Innovate Healthcare. About Roche
Headquartered in Basel, Switzerland, Roche is one of the world’s leading research-focused healthcare groups in the fields of pharmaceuticals and diagnostics. As the world’s biggest biotech company and an innovator of products and services for the early detection, prevention, diagnosis and treatment of diseases, the Group contributes on a broad range of fronts to improving people’s health and quality of life. Roche is the world leader in in-vitro diagnostics and drugs for cancer and transplantation, and is a market leader in virology. It is also active in other major therapeutic areas such as autoimmune diseases, inflammatory and metabolic disorders and diseases of the central nervous system. We now seek to recruit an Experienced Medical Writer to join our team in Welwyn Garden City, UK. This is an excellent opportunity to be at the heart of the drug development and licensing process — taking responsibility for key documentation projects and driving them through to fruition. As part of the Pharmaceutical Development division of Roche, you'll also be working at the leading-edge of the pharmaceutical industry, helping to bring important new medicines to market. Your role will be to plan and to write key clinical regulatory documents (including clinical study reports, investigator brochures, clinical summaries and overviews), ensuring that they meet the highest standards of quality, accuracy and organisation. As a key member of global project teams you will be working closely with statistical, scientific and medical associates to plan data tabulations, review and interpret data, draft documents, accommodate feedback and ensure that all aspects of clinical NDA/MAA documentation are adequately planned and executed. Together with a PhD, MSc or equivalent in a biomedical discipline, you will need to have previous medical writing experience and to demonstrate a clear, concise scientific writing style. Equally important will be your flexible approach, attention to detail, and the ability to work on a variety of projects and documents within schedule across different therapeutic areas. Previous experience of clinical research and development in a pharmaceutical company would be a major asset, particularly if this included involvement in the preparation of high level clinical summaries and in regulatory filings.
It's a globally focused, highly challenging role, where you will take responsibility for your own project within a supportive, close-knit team. So, it calls for a detail-conscious, persuasive, influential and decisive approach, with a talent for cross-culture communication. In return Roche offers a competitive salary plus the excellent benefits you would expect from a blue-chip organisation, including a genuine interest in your development and progression, together with a modern, state-of-the-art office environment. To be considered for this position, please apply at http://careers.roche.com/uk. When completing your application, please ensure you attach an up to date CV and details of your current remuneration package. |
Placed 12/04/08 | PRISM IDEAS Positions available: South Cheshire Medical Marketing Consultancy seeks leading Regulatory Medical Writer with initiative Location: Nantwich, Cheshire Salary: Competitive remuneration package available Who we are: A dynamic and expanding Medical Consultancy and Communications agency with a broad client base. We operate a non-hierarchical editorial team and offer excellent future career prospects in an informal, friendly working environment. The role: We are looking for a high calibre Regulatory Medical Writer who has the flexibility to work on a range of projects over several therapy areas. The individual: The successful candidate should have 1–6 years’ agency experience of producing a range of high quality regulatory materials. He or she will posses excellent written/oral communication skills, while being organised, flexible and a good team player. Attention to detail is essential. To apply: Send a CV and covering letter to Dr Colin Hayward, Prism Ideas Ltd, Regent House, Princes Court, Beam Heath Way, Nantwich, Cheshire, CW5 6PQ
Or, electronically to
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(www.prismideas.com) |
Placed 3/04/08 | FREELANCER NEEDED An established medical publishing firm functioning as the publishing arm of a larger medical education/communications company has is an opportunity for an experienced medical writer to attend assigned sessions at the European Congress of Microbiology and Infectious Diseases (ECCMID) in Barcelona Spain between April 19-22……..Will capture key content and write three -four articles totaling app. 3,000 words (range between 300 and 1,000 words per article) for a medical newspaper, Conference Perspectives. Specific direction and guidance will be provided in advance, including specific objectives of each article……Must be experienced in medical news reporting (different from peer-reviewed journal writing) and be familiar with current AMA writing style…….Writers will be responsible for submitting all completed manuscripts electronically, within three days (72 hours) of the official completion of the conference……. Must also send by overnight courier all support materials (official conference program, presentation slide decks, presentation hand outs, “permissions to use”, audio tapes, reference materials, hard copies of each written manuscript, suggested figures and tables, annotated meeting materials) to also arrive to Dothen editor no later than 72 hours following official completion of the conference.…….Writers will be compensated at the rate of $1.00 (US) per word plus $100 (US) per diem for each day attending sessions. Partial relief for travel expenses will be considered……. Interested parties should respond to
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with attached resume, writing samples (especially on infectious diseases), and your thoughts on why you think you’ll be a good fit for this assignment. Martin Zittel President/Publisher
Dothen Healhtcare Press
A Strategic HealthCOM Company
25 Lindsley Drive, Suite 208
Morristown, NJ 07960
USA |
Placed 16/04/08 | 
Medical Writer or Senior Medical Writer
Based near Oxford Doctors.net.uk is an exciting and successful Internet-based service, exclusively for UK doctors and medical students. With its unrivalled access to 153,000 doctors, it is also a leading provider of online sales and marketing services to the pharmaceutical industry. We are looking for a medical writer to be part of the team responsible for the delivery of pharmaceutical campaigns to doctors and to take responsibility for the writing of content. In this role you will work closely with account managers, designers, medical advisors, and the business development group. Specific responsibilities include: - Interpreting and transforming customers’ medical and marketing materials into effective online content
- Liaising directly with pharmaceutical customers and opinion leaders
- Interviewing opinion leaders
- Reporting news and clinical developments from international conferences
- Writing medical education for primary and secondary care doctors
- Conducting background research to develop a full understanding of the brief and the subsequent content of the campaign
- Reviewing market research data and clinical and marketing materials
- Proofreading all documents prior to submission to the customer
- Providing research and ideas to the Business Development team
Qualifications/requirements: - Background in medicine or life sciences
- Substantial medical writing experience, preferably in the commercial sector
- Ability to present clinical/medical data to the medical profession in an attractive and effective style
- Willingness to travel
- Ability to work on a range of projects at the same time
- Excellent writing and proofreading skills
Initial six-month contract with possibility to extend.
Salary: £excellent. www.doctors.net.uk/marketing Please apply by email to
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with your CV. Please include details of the notice period required in your current position. |
Placed 1/04/08 | 
Department : Clinical Development Clinical Writer Location : Corporate (Lyon) Mission :
To manage all areas of the Sanofi Pasteur MSD Clinical Design and Evaluation Team with regards of writing and editing clinical/scientific documents in order to support the clinical projects teams (Corporate and regions) in delivering timely and quality clinical documents in accordance with ICH-GCP, regulatory requirements, and Company policies and procedures. Environment :
To achieve the responsabilities below, the Clinical Writer will need to liaise with the rest of the Clinical Development Department as well as with other Departments: - Regulatory
- Legal
- Medical Affairs, including Medical Services
- Pharmacovigilance & Risk Management
- Sanofi pasteur and Merck
- Contract Research Organisations
Responsibilities :
Under supervision of the Clinical Design and Evaluation Management : - Prepare or support preparation of clinical study concept sheets, protocols (including amendments) and reports (including appendices), and any clinical documents (such as those for Clinical Trial Application, submission to Ethics Committees or to Health Authorities) in collaboration with the other teams
- Ensure all documents are well-organised, accurate, consistent within and across documents for style, format and content, and in compliance with applicable Company policies and regulations
- Participate in summarizing data from clinical studies to draw a conclusion
- Ensure archiving of clinical study reports and any other clinical documents is well-organised and complete
- Perform literature research
Other Responsibilities : - Keep up to date on relevant technical and regulatory environment on medical/clinical writing
Necessary skills : - Ability to work precisely according to procedures, rules and regulations
- Good grasp of ICH and EMEA requirements and guidelines for clinical protocols, clinical study reports, and clinical documents for regulatory submissions
- Excellent writing skills
- Ability to summarize data to draw a conclusion
- Systematically perform activities in a timely, accurate and quality manner
- Ability to work self-sufficiently as well as collaboratively with the other teams
- Ability to work in an international and multifunctional environment
Technical knowledge : - Excellent writing and verbal communication skills
- Excellent English level (writing and/or speaking) Ideally, English-native speaker
- Excellent computer skills and experience using Word, Adobe Acrobat and style guides, ECSR
Thank you to send your application to:
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(Reference: Clinical Writer) Website: www.spmsd.com |
You too can have an advert: click here for details. Placed 23/03/08 | nspm ag
is a successful medical communications company located in Switzerland. We implement clinical and marketing projects for international customers in the pharmaceutical industry. nspm provides a complete medical writing service across a broad spectrum of therapeutic areas, with the experience and expertise of its highly qualified in-house medical writers. For our team we are currently looking for a SENIOR MEDICAL WRITER YOUR PROFILE - University degree and higher education (PhD/MD) in medicine, natural or health sciences, or pharmacy
- English mother tongue
- At least two years experience in writing clinical and regulatory documents
- Computer literacy (PowerPoint/Word)
YOUR MAIN RESPONSIBILITIES - Writing and editing medical texts, including
- clinical study protocols and reports
- drug submission dossiers
- manuscripts and abstracts
- slide presentations
- Organising scientific symposia and meetings
We offer a stimulating job in a dynamic team environment. If you are interested in a challenging position in the heart of Switzerland, please send your CV by e-mail to
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If you require further information, please call
Dr. Ian Leighton on +41 41 377 53 41 nspm ltd, Luzernerstrasse 36, CH-6045 Meggen, Switzerland | |
Placed 19/03/08 |  Clinical Writer Up to £30K, Swindon, UK based Catalent Pharma Solutions is the leading provider of advanced technologies, development manufacturing and packaging services for pharmaceutical and biotechnology, as well as consumer health companies, in nearly 100 countries. Employing approximately 10,000 people at more than 30 facilities worldwide, we generate more than $1.7 billion in annual revenue. Working within our Regulatory Department at Swindon, you will write a variety of study related documents including protocols, Investigational Medicinal Product dossiers, clinical study reports, journal manuscripts and clinical summaries. Writing and reviewing Patient Information Leaflets (PILs) and participating in PIL user testing will utilise your skills and your technical knowledge and strong command of English. Well-developed communication skills will help you build strong working relationships with both internal and external clients as you communicate regularly on project issues. Making full use of previous pharmaceutical industry experience as a medical writer, you will work within SOPS and ICH regulatory guidelines and get involved in the quality control of a range of documents produced by other members of the Department. You will need a pharmacy, medical related or life science degree plus specific knowledge of writing clinical study related documents including clinical study reports and protocols. A good grasp of MS Office is essential. Ideally you will also have completed the EMWA Professional Development Programme at a basic level. To apply please send your CV along with details of your current salary to David Rowlands, HR Manager, Catalent Pharma Solutions, Frankland Road, Blagrove, Swindon, UK or via e-mail to
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. Closing date: 7 April 2008 No agencies please. |
Placed 1/03/08 | Senior Writers for European Gateway Office in Ireland
Clinical, CMC, Pharmacovigilance Synchrogenix Ireland is a new subsidiary of Synchrogenix Information Strategies. With 22 years of success in the global pharmaceutical industry, Synchrogenix is seeking senior writers with expertise in clinical, CMC, and pharmacovigilance to work in our new office. We chose Ireland for our European base because of the quality of life it offers. Concern for our employees’ quality of life affects all our business decisions. Synchrogenix is a writing company run by writers for writers.
We’re proud that our employees say we have the most supportive and rewarding workplace environment they have encountered. And by hiring responsible professionals with a strong work ethic, we can offer them the flexibility they need to manage their lives outside of work.
We have cultivated a non-hierarchical organization, in which every employee participates in decision-making and has the opportunity to try out leadership roles. Every employee, from the newest university graduate to the most senior regulatory expert, has something to learn and something to teach. By participating as both teacher and student, we all grow and learn together. Our senior writers are responsible for writing strategic documents and managing writing projects, including oversight of editing and quality control. They organize and manage multiple tasks related to regulatory documents and ensure that timelines and budgets are met, and documents are completed according to applicable standards, regulations, and guidance. Applicants should have strong regulatory writing experience with key documents, the ability to mentor junior writers and to lead concurrent projects, and strong client management skills. Clinical writers should have experience with: - Writing clinical documents per ICH guidelines
- Clinical study design and protocol development
- Management/development of INDs, IBs, and/or agency response documents
CMC writers should have experience with: - Pharmaceutical manufacturing and laboratory analysis
- QA
- CGMP
- Process validation
Pharmacovigilance writers should have experience with: - Pharmacovigilance process development
- Risk management plan development and associated activities
- Signal detection requirements
- Statistical analysis and interpretation
- Post-marketing studies and reporting, and/or
- Promotional labeling and advertising regulations
Send your CV to
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Placed 28/02/08 | Our client is the Swiss-based International Headquarters of one of the world’s most prominent biotechnology companies, with the corporate mission to be the world leader in discovering, developing and delivering important and highly innovative human therapeutics. On behalf of our client, we are seeking the Scientific Publications
Senior Manager (m/f) In this high impact position you play a pivotal role in the publication of key clinical and scientific data for the company’s marketed and pipeline breakthrough biotech therapeutics. You will be responsible for the strategic publication planning and execution in the international region; that includes the preparation of a scientific publication plan and the execution through a combination of own writing and outsourcing. You will work closely with a crossfunctional medical affairs team as well as with external authors and investigators. You will also hire and supervise external vendors and contractors to assist you in the preparation of publications materials. To meet the requirements of this Global Leader company, you have a degree in life sciences (PhD or MSc) and several years experience in publications writing and management within the pharmaceutical industry or in a medical communications agency. You demonstrate superb medical writing in English, excellent communication and managerial competence, combined with outstanding project management capabilities. In addition to this, you are proficient at multitasking, capable of coordinating and leading complex writing projects simultaneously, and able to successfully work in an international matrix environment. Interested candidates are invited to submit their CV, letters of reference/recommendation and photo. Your application will be treated with strict confidentiality. Ms Regina Sager-Desserich
MA Law
direct dial: +41-61-261 94 17
Gerbergässlein 41
CH-4051 Basel
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www.pp-pharma-plan.com |
Placed 25/02/08 | Prism Ideas Positions available: South Cheshire Medical Marketing Consultancy seeks leading Medical Writers with initiative Location: Nantwich, Cheshire, UK Salary: Competitive remuneration package available Who we are: A dynamic and expanding Medical Consultancy and Communications agency with a broad client base. We operate a non-hierarchical editorial team and offer excellent future career prospects in an informal, friendly working environment. The role: Want to cut out the middle-man? We are looking for high calibre Senior/Principal Medical Writers who have the flexibility to write on a range of projects, fulfilling a multi-functional role by leading their own accounts and interacting directly with our clients. The individual: The successful candidate should have 1–6 years’ agency experience of producing high quality medical communications. He or she will posses excellent written/oral communication skills, while being organised, flexible and a good team player. Attention to detail is essential. To apply: Send a CV and covering letter to Dr Colin Hayward, Prism Ideas Ltd, Regent House, Princes Court, Beam Heath Way, Nantwich, Cheshire, CW5 6PQ
Or electronically to
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(www.prismideas.com) |
Placed 6/02/08  | Envision Pharma has clients across the globe and offices in the UK and USA. With a range of unique scientific and cutting-edge technology solutions including Datavision™, we are market leaders in medical communications. Due to significant expansion we have opportunities for medical writers which offer exciting challenges in a vibrant environment. Innovation is at the heart of everything we do. To make your mark you will need a proven track record of medical writing and editing, backed by an exceptional eye for detail. Ideally, you will have a relevant higher degree and have worked in a medical communications agency (or equivalent). Using your initiative to the full, you will research, write, edit and proof copy to the highest scientific and grammatical standards. There will be plenty of variety, as you will work on the full spectrum of educational materials from manuscripts and posters to slide kits and product monographs, and you will also play a central part in managing projects, liaising with clients and implementing amendments. We are a dynamic and rewarding company to work for with excellent benefits, including home working, and an informal friendly working environment with the opportunity to live and work in the USA. Please e-mail your CV to
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.com alternatively visit www.envisionpharma.com for the latest career opportunities. | |
Placed 5/02/08 | 
The Agency, based in London, is responsible for co-ordinating the evaluation and supervision of medicinal products for human and veterinary use in the European Union. Further information on the EMEA and its activities is available on the website: www.emea.europa.eu The EMEA is recruiting (m/f) - Head of Sector for Pharmacovigilance and Risk Management of Medicinal Products for Human Use
- Scientific Administrators (pharmacists, physicians, health professionals) with experience in medical writing/quality of medicines/pharmacovigilance/pharmaceuticals in a regulatory environment
Candidates must be nationals of a Member State of the European Communities, or of Iceland, Liechtenstein or Norway. Conditions and essential requirements are available on the EMEA website: www.emea.europa.eu Detailed job description, conditions and essential requirements, together with the electronic application form, which must be used, are available on the EMEA website at : www.emea.europa.eu/htms/general/admin/recruit/recruitnew.htm The deadline for receipt of applications is midnight on 18 March 2008. EMEA - 7 Westferry Circus, Canary Wharf, UK-London E14 4HB
(Tel.: + 44 20 7418 8400 - Telefax: + 44 20 7418 8416). | |
Placed 4/02/08 | Our client is a highly respected Medical Communications Agency believes in using leading-edge expertise and strategic thinking to deliver powerful global medical Communications programmes. They believe firmly that continued success in delivering unparalleled client service and distinctive quality lies in its ability to improve its team through developing the capabilities and strengths of individual team members. They work with some of biggest names in healthcare and across a spectrum of brands – from primary care blockbusters through to specialist niche brands. They are proud of the fact that many of their client relationships are well into their second decade and still going strong. They are also firm believers in new business and there continued success in winning new business has aided their continued growth. They are committed to ensuring that they offer a successful and rewarding place to work – for their team members and clients alike. Editorial Team Leader - London A fantastic opportunity has arisen for an Editorial Team Leader in London to work on a major cardiovascular account, managing internal writers’ resource allocation and editorial quality & process. You will have extensive skills in writing editing and editorial management within a medical communications agency Senior Medical Writer – London (office) or home based nationwide You will be writing on a senior level. You must be enthusiastic and a real team player. You should be able to review the work, mentor and develop junior medical writers. Good publication planning experience as well as proficient skills in working with Key Opinion Leaders on slide production for international congresses. For more information or for an informal discussion please contact Jennifer Harris
+44-1273-727-930 or email
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Placed 4/02/08 | INNOVATIONS IN VIROLOGY -
Unique therapies against viral infectious diseases and cancer AVIR Green Hills Biotechnology
is a biopharmaceutical company based in Vienna, Austria. AVIR Green Hills Biotechnology uses its know-how in virology to develop and commercialize innovative products that offer cost-effective treatment for a wide range of diseases. The products under development are unique therapies against viral infectious diseases and cancer with the aim to significantly improve health and the quality of life of human beings. Due to continued growth we are now seeking an experienced Medical and Scientific Writer (m/w)
(office based) who will be primarily responsible for generating high-quality documents that meet scientific and regulatory requirements. Your responsibilities: - Collaboration with internal scientists and external contract laboratories on the writing of preclinical study reports
- Writing of clinical study reports and other clinical documentation according to the relevant guidelines
- Generation of manuscripts for scientific articles
- Conducting background research and literature reviews to help with document preparation
- Proofreading/editing the work of other writers as requested
- Summarising relevant data and information for documents such as Investigators Brochures
Your skills and experience: - MD, Pharm D or Life Science degree
- Experienced in writing and editing of reports and documents if scientific and medical research
- Excellent English skills
- Computer proficiency
- Knowledge of regulatory requirements
- Experience in Biotechnology sectors preferred but not required
Personality: reliable, well structured and organised, self-confident, flexible, team-spirit, diligent. If you are interested in joining our young and enthusiastic team in the development of innovative medicines, please send your letter of application and CV to Green Hills Biotechnology
A-1180 Wien, Gersthofer Strasse 29-31, Tel: 01 319 96 70 Fax: 01 319 60 99
www.greenhillsbiotech.com Contact:
Isolde Bergmann (HR & CC)
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Placed 30/01/08 | Pharmaceutical company near Paris–La Défense, France, offers challenging position at the crossroads of medical publishing, editing, and writing, for a confirmed: MEDICAL EDITOR MD, PharmD, PhD We are: A leading dynamic and internationally expanding innovative French pharmaceutical company, with research and business activities focused on the cardiovascular, metabolic, neurosciences, and other fields. Our headquarters are located near Paris–La Défense, France. Your role: You will join an international editorial team within a full-scale in-house medical publishing department, and work in a stimulating and convivial environment. The position involves rewriting, checking, copyediting, and proofreading pharmaceutical and medical literature in English, to the highest scientific and grammatical requirements. You will work in close cooperation with the international product managers, internal and external authors, and graphic designers and publishing project managers, to ensure timely preparation and enhance the form, presentation, and quality of a comprehensive spectrum of publication and document formats relating to our drugs, across all stages of the editorial process, in accordance with our house style and standard procedures. Your profile: You are preferably an MD or a pharmacist, or have a PhD in life sciences. You have experience in medical editing and writing, preferably within the pharmaceutical industry and across several therapeutic areas, as well as the ability to learn quickly. Your English speaking and writing skills commensurate with those of a native English speaker. You have a keen eye for detail and a passion for the precise word and phrase, clear and effective communication, and fact checking and finding. You are well organized, computer-literate, and able work to strict timelines on several projects simultaneously. You are able to build excellent working relationships both within and without the company and function within a team. A working knowledge of French would be an advantage. Valid EU working papers are essential. Salary: Full-time position with an attractive salary package and pension scheme. To apply: Send a detailed curriculum vitae and covering letter stating your reasons for interest in this position and current salary package, to PUBLIVAL/2013
27 route des Gardes, 92190 MEUDON (France) or
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Placed 24/01/08 | 
Medical Writing Specialist Gilead Sciences is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet need. With each new discovery and experimental drug candidate, we seek to improve the care of patients suffering from life-threatening diseases. Gilead’s primary areas of focus include: antivirals (e.g., HIV/AIDS, chronic hepatitis), cardiovascular conditions (e.g., pulmonary arterial hypertension, resistant hypertension) and respiratory diseases (e.g., influenza, cystic fibrosis). We are seeking a medical writing specialist to support our International Regulatory Group with respect to regulatory report, summary, and response writing. Job Requirements
Prepares documents such as clinical study reports and investigator brochures in line with regulatory requirements and Gilead internal document standards. Deliverables such as single study reports and noncritical documents are prepared without appreciable supervision. Prepares more complex regulatory documents (e.g., CTD summaries, regulatory responses) with direction from Associate Director/Director. Contributes to other non‑regulatory medical writing activities. Participates in submission teams, providing advice/guidance for optimal data presentation to achieve document objectives. Leads document timeline/resource planning within the submission team. Works collaboratively with functional contributors (clinical, biometrics, virology etc), ensuring all source information/data are appropriately reported in terms of accuracy, completeness and scientific interpretation, and in accordance with project timelines. Coordinates the compilation of final documents and appendices. Contributes to development of document standards, templates, and other aspects of document management. Participates in group and somewhat complex Company-wide process improvement and development initiatives. Knowledge
Demonstrated success in the preparation of regulatory documents, particularly at the individual study report level. Highly developed and proven medical writing skills. Excellent verbal communication skills. Knowledge of regulatory document requirements/guidelines. Understands somewhat complex document management, authoring and publishing tools, and their applicability for workflow efficiency. Well-developed computer skills including proficiency in Word, Powerpoint and Excel. Use of project management tools and graphics packages also desirable. Education and Experience
Typically requires a BA/BSc and extensive relevant experience within clinical R&D or regulatory affairs, including experience in a medical writing environment preparing documents for regulatory submissions. This is a UK‑based opportunity. To apply, or for more information, please contact: Lucia Fernandez
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01223 897 314
www.gilead.com |
Placed 16/01/08 
CSL Behring is a global leader in the plasma protein biotherapeutics industry, dedicated to treating rare and serious diseases and passionate about improving the quality of life of patients throughout the world. CSL Behring employs more than 7,000 people worldwide, thereof approximately 1,900 people in Germany. The company's largest manufacturing and research site is located in Marburg. | For our Marburg site (Germany) we are currently looking for the role of a Medical Writer (f/m)
(Medical Writing and Document Management) In this in-house position you are responsible for providing scientific and related medical writing expertise regarding clinical research for investigational drugs in the field of plasma products for the CSL Behring Clinical Research & Development (CRD) organization. Responsibilities: - Preparation of regulatory and study related documents including study protocols, investigator brochures, study reports and CTD documents.
- Management of external medical service providers and resource planning.
- Participate in the preparation of responses to regulatory agencies.
- Review of publications, abstracts, and posters.
- Develop writing tools such as style manuals and templates. Take primary responsibility for clinical document template creation, use and maintenance.
Qualifications and Competencies: - Degree in natural science, preferably with a PhD; or with education in natural sciences.
- Experience in medical writing, ideally in the indications immunology, hematology, or neurology.
- Excellent level of English language proficiency, both written and spoken.
- Expert MS Office skills with a special focus on word processing, tables and graphics, spreadsheets,
- presentations and templates.
- Flexibility to work independently and within a team.
- Excellent communication and interpersonal skills and ability to maintain working relations both internally and externally.
If you are interested in this challenging career opportunity, please send your CV and application form to Inga
Koradin.
CSL Behring GmbH
Human Resources Marburg
P.O. Box 1230, D-35002 Marburg
E-Mail:
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Placed 11/01/08 | 
MEDICAL WRITER/SENIOR MEDICAL WRITER - OFFICE AND HOME BASED !!! Established in 1982, Chiltern is a leading global Contract Research Organisation with extensive experience of running and staffing international Phase I to Phase IV clinical trials across a broad therapeutic range for a wide variety of clients. Chiltern employs more than 1100 people with 20 offices across the United States, Europe and in India. Chiltern provides services including Early Phase, Global Clinical Development, Late Phase, Biometrics, Medical and Regulatory Affairs and Resourcing Solutions. Due to our continuing success and expansion, we are looking to recruit an Experienced Medical Writer. As a Medical Writer you will work as part of a dynamic, friendly team in an attractive, unique office environment, supported by experienced colleagues from different disciplines. In return we offer excellent remuneration and training opportunities, and the chance to join in subsidised social events.
There is the option to be office based or to work from home.
Responsibilities: - Preparation of clinical study reports, expert reports, clinical summaries, and periodic safety update reports for a wide variety of therapeutic indications.
- Production of manuscripts for submission to peer-review journals.
- Production of patient safety narratives.
- Preparation and review of study protocols.
- Attendance at client meetings and participation in multidisciplinary teams.
- Production of high quality documents in compliance with regulatory requirements.
- Advising colleagues and clients on medical writing-related issues.
- Opportunity to mentor more junior writers.
Profile: - Life-science graduate with previous medical writing experience in a clinical trials environment or similar. An MSc or Ph.D in a life science is also desirable.
- Excellent written and spoken English, able to accurately interpret data and express findings in a clear and concise manner, and excellent word processing skills and knowledge of Microsoft WORD.
- Good knowledge of ICH-E3 and ICH-E6 guidelines.
For a confidential and informal discussion about this opportunity, please phone our Internal Recruiter Steven Dilworth on +44 (0)1753 216 674. To apply, please send your CV to
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Placed 10/01/08  | he Medical Information Department at Prous Science, a Thomson Scientific company, is looking for candidates to expand our portfolio of free-lance medical writers in Spanish and English. If interested, please, send details with a CV to
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for an initial test for suitability. | |
Placed 10/01/08 | nspm ag
is a successful medical communications company located in Switzerland. We implement clinical and marketing projects for international customers in the pharmaceutical industry. nspm provides a complete medical writing service across a broad spectrum of therapeutic areas, with the experience and expertise of its highly qualified in-house medical writers. For our team we are currently looking for a MEDICAL WRITER / PROJECT MANAGER YOUR PROFILE - University degree and higher education (PhD/MD) in medicine, natural or health sciences, or pharmacy
- English mother tongue
- Editorial or medical writing experience in the pharmaceutical industry is desirable
- Computer literacy (PowerPoint/Word)
YOUR MAIN RESPONSIBILITIES - Writing and editing medical texts, including abstracts, publications and slides
- Proofreading texts
- Organising scientific symposia and meetings
We offer a stimulating job in a dynamic team environment. If you are interested in a challenging position and working in the heart of Switzerland, please send your CV by e-mail to
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If you require further information, please call
Dr. Ian Leighton on +41 41 377 53 41 nspm ltd, Luzernerstrasse 36, CH-6045 Meggen, Switzerland | |
Placed 2/01/08 | Regulatory Documentation Specialist Position, Plus Maternity Cover Welwyn Garden City, Herts This is an excellent opportunity to be at the heart of the drug development and licensing process — taking responsibility for key documentation projects and driving them through to fruition. As part of the Pharmaceutical Development division of Roche, you'll also be working at the leading-edge of the pharmaceutical industry, helping to bring important new medicines to market. Major responsibilities in this key role include producing clinical regulatory documents, (including clinical study reports, investigator brochures and CTD Module II summaries) to the highest standards of quality, accuracy and organisation. Working as part of global multifunctional teams, you will also provide input into statistical analysis plans, review and interpret data, accommodate feedback and ensure that all aspects of clinical documentation are adequately planned and executed. Together with a PhD, MSc or equivalent in a biomedical discipline, you will need to have previous medical writing experience and to demonstrate a clear, concise scientific writing style. Equally important will be your flexible approach, attention to detail, and the ability to work on a variety of projects and documents within schedule across different therapeutic areas. Previous experience of clinical research and development in a pharmaceutical company would be a major asset, particularly if this included involvement in the preparation of high level clinical summaries and in regulatory filings. It's a globally focused, highly challenging role, where you will take responsibility for your own project within a supportive, close-knit team. So, it calls for a detail-conscious, persuasive, influential and decisive approach, with a talent for cross-culture communication. In return Roche offers a competitive salary plus the excellent benefits you would expect from a blue-chip organisation, including a genuine interest in your development and progression, together with a modern, state-of-the-art office environment. In addition, we are seeking someone to provide maternity cover for an analogous position, some of which will be office-based. To be considered for either of these positions, please apply at http://careers.roche.com/uk. When completing your application, please ensure you attach an up to date CV and details of your current remuneration package. |
Placed 11/12/07 | nspm ag
is a successful medical communications company located in Switzerland. We implement clinical and marketing projects for international customers in the pharmaceutical industry. nspm provides a complete medical writing service across a broad spectrum of therapeutic areas, with the experience and expertise of its highly qualified in-house medical writers. For our team we are currently looking for a SENIOR MEDICAL WRITER YOUR PROFILE - University degree and higher education (PhD/MD) in medicine, natural or health sciences, or pharmacy
- English mother tongue
- At least two years experience in writing clinical and regulatory documents
- Computer literacy (PowerPoint/Word)
YOUR MAIN RESPONSIBILITIES - Writing and editing medical texts, including
- clinical study protocols and reports
- drug submission dossiers
- manuscripts and abstracts
- slide presentations
- Organising scientific symposia and meetings
We offer a stimulating job in a dynamic team environment. If you are interested in a challenging position in the heart of Switzerland, please send your CV by e-mail to
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If you require further information, please call
Dr. Ian Leighton on +41 41 377 53 41 nspm ltd, Luzernerstrasse 36, CH-6045 Meggen, Switzerland | |
Placed 11/12/07 |  With around 100,000 employees, sanofi-aventis is one of the world’s leading research-based pharmaceutical companies and is No. 1 in Europe. Our core therapeutic areas: cardiovascular disease, thrombosis, oncology, diabetes/metabolic disorders, central nervous system and internal medicine. And to prevent diseases, sanofi-aventis also develops vaccines. The 10,000 people who work for the sanofi-aventis Group in Germany perform basic research and development, produce active ingredients, and manufacture and market medicinal products. In so doing, we promote Germany as a business location and improve medical care for people everywhere.
The Pharmaceutical Development Department in Frankfurt/Germany has an opening for a (Senior) Medical Writer (f/m) initially on a contract limited for 12 months. Your role
As an integral part of international teams with members located around the world, you will support the clinical development of drug candidates in a broad range of therapeutic indications. Ensure the quality, standards compliance, and timely production of English language regulatory documentation for the initiation and reporting of clinical studies. In addition to contributing hands-on medical writing skills, you will manage the authorship, approval, and QC processes. Senior applicants will also manage the preparation of dossiers supporting marketing applications and act as mentors for junior associates. Your profile
You have experience in the compilation of all types of English-language regulatory documentation. Have excellent oral and written English skills and have experience expressing medical data accurately and concisely. You are a team player with excellent communication, problem-mediation, and organizational abilities. Meticulous, proactive, deadline orientated, have good MS-word skills, and ideally have experience with e-documentation management systems. You have a life sciences degree, preferably a PhD or MD. Knowledge of German would be an advantage. What we offer
In addition to a varied and interesting job in a competent and well-established team within an international company, we offer an attractive salary commensurate to your qualifications with an above-average compensation package as well as considerable support for your further professional and personal development. If you would like to be considered, please send a resume indicating your full career history and current employment details preferably online at www.sanofi-aventis.de/karriere or apply to the address below.  Sanofi-Aventis Deutschland GmbH
Human Resources Recruitment & Marketing • Industriepark Höchst • Gebäude H 831 • D-65926 Frankfurt am Main
www.sanofi-aventis.de/karriere |
Placed 7/12/07 |  Avec 1.200 collaborateurs, GUERBET - Groupe Pharmaceutique International - est un acteur majeur en imagerie diagnostique au niveau mondial et réalise un ca de 290M€ en 2006 dans 70 pays. Notre croissance permanente et notre recherche de performance nous conduisent à accélérer notre développement en recherchant notre : COORDONNATEUR REDACTION MEDICALE (poste basé en région Parisienne) I - LE POSTE Au sein du siège mondial et sous le Responsable des Opérations Cliniques, au sein du Département Développement Médical, vous avez en charge la responsabilité de la coordination de la rédaction médicale ainsi que la gestion de la sous-traitance de cette activité. A ce titre, vous : - Travaillez en collaboration étroite et de façon transversale avec les chefs de projets du département pour les études cliniques, de leur préparation au rapport, en leur apportant votre expertise de la rédaction médicale : planification, coordination et réalisation des documents nécessaires.
- Rédigez des articles scientifiques pour soumission à des revues référencées et organisez le circuit de relecture externe et interne.
- Participez à l'élaboration de la partie clinique des dossiers d'AMM, en assurant le respect du cadre réglementaire et des échéances (CTD parties 2.5, 2.7 et 5).
- Constituez les brochures investigateurs, les rapports d'études selon les normes ICH, et les rapports annuels de sécurité.
- Répondez aux questions cliniques des autorités sur les produits commercialisés.
- Effectuez les recherches bibliographiques préalables nécessaires.
II - LE PROFIL DU CANDIDAT RECHERCHE De formation scientifique supérieure (Sciences biomédicales et/ou Pharmaceutiques), vous avez une expérience opérationnelle réussie d’au moins 5 années dans la rédaction médicale dans l’industrie pharmaceutique. Cette expérience s’est impérativement déroulée dans un contexte international.
Votre expérience de la réglementation pharmaceutique internationale et votre connaissance des essais cliniques, de leur conception au rapport, font de vous un interlocuteur reconnu.
Vos capacités de communication vous permettent de travailler en concertation avec des interlocuteurs divers (internes et externes).
Ouvert d'esprit et diplomate, vous disposez d’un vrai sens du service, d'excellentes qualités relationnelles et avez déjà fait la preuve de votre capacité à travailler en équipe.
Anglais courant exigé. Merci d’adresser CV + rémunération actuelle, sous réf : 07-140-01/EMWA à ALERYS
Par mail à
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Placed 23/01/08  | We are a national body, working with health care professionals and the public to improve the quality of health services in Scotland. Medical Writer
£23,458 - £31,779 (Band 6)
1 year fixed term (Maternity Cover)
Edinburgh or Glasgow (Ref: PR180/EMW) Working within a variety of multidisciplinary project teams, you will support the production of national Health Technology Assessments, Evidence Notes and a variety of other printed and electronic communications. You will be educated to degree level in a life sciences field or hold commensurate experience. Experience of writing and editing large-scale scientific publications and formal reports is essential together with experience of writing for a lay audience. European Medical Writers Association (EMWA) accreditation is desirable. This may represent a secondment opportunity for suitable candidates. Closing date for this first post: 4th February 2008 Medical Writer
£23,458 - £31,779
1 year fixed term (Maternity Cover)
Edinburgh or Glasgow (Ref: PR180/EMW2) Our Medical Writers work within multidisciplinary project teams and support the production of national Health Technology Assessments, Evidence Notes and a variety of other printed and electronic communications. The role represents an excellent opportunity to invest your experience in writing/editing large-scale scientific publications and formal reports with the need to keep lay audiences engaged. European Medical Writers Association (EMWA) accreditation is desirable but not essential. For more information about the role and closing date
email:
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email:
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Tel: 0131 623 4590 Textphone: 0131 623 4383 www.nhshealthquality.org Committed to equal opportunities | |
Placed 18/01/08  | | Looking for a fresh opportunity? Information Transfer is a communication and training consultancy working in many sectors, but with a firmly established reputation as a niche supplier of effective, original training materials to the pharmaceutical and healthcare industries. We have long-standing relationships with clients who value our scrupulous attention to detail and excellent writing and communication skills, and who prefer the personal attention that we offer a small number of clients to the “large agency” approach. We are looking for an outstanding medical writer to join us. We offer the satisfaction of stimulating work performed to a high standard, and direct involvement with clients. As a member of a small team you will have the potential to influence the development of our pharmaceutical business and to contribute to and share in its success. If this is the opportunity you are looking for, we’d like to hear from you. Please download the application pack, which includes a written test, from the pdf icon beneath this advertisement. The closing date for applications is 4 February 2008.  Information Transfer LLP
Burleigh House
15 Newmarket Road
Cambridge CB5 8EG, UK Tel: +44 (0)1223 312227
www.informationtransfer.com | | More details |
