EXPERIENCED MEDICAL WRITERS
MMS is a global pharmaceutical service organization (CRO) that focuses on regulatory submission support for the pharmaceutical, biotech and medical device industries. We support pharmaceutical and biotech industries with medical writing, biostatistics, clinical programming, data management, clinical development, regulatory affairs, regulatory submissions and pharmacovigilance.
Our mission is to deliver high-quality services, rooted in good science and decades of regulatory experience, which will assist our clients in developing and marketing life-changing therapies, thereby positively affecting patients' lives worldwide.
Due to ongoing expansion, we are looking to recruit a number of experienced medical writers on either a freelance or permanent basis. Document types involved will be CSRs, CTD modules 2.5 and 2.7 as well as safety documents. Roles can be home based in the US or Europe, or be based from our HQ in Canton, Michigan. At present we are looking for candidates who can work full time hours. Unfortunately we cannot consider applicants looking for part-time hours.
How to apply:
To be considered for these opportunities, please send your CV to Matt McGinley at firstname.lastname@example.org