Medical Writer - I

The Medical Writer Specialist is responsible for preparing documents that support the presentation and/or publication needs of assigned therapeutic areas and/or medical devices. Primarily focuses on preparing, writing, editing, and reviewing regulatory documents and responses to regulatory authorities. Participates in post-market surveillance activities by conducting routine systematic literature reviews and prepares summaries into formal reports.

Requirements

• Ph.D/Pharm D plus 1 to 2 years of related medical device/drug industry experience
• BS/B.Pharm/BSN or MS or MPH plus 4 to 5 years of relevant medical device/drug industry experience
• Excellent English language skills, especially writing and proofreading
• Clinical, scientific or research background, highly preferred
• Experience writing CERs, highly preferred
• Knowledge in narrative or systematic literature reviews (e.g. PRISMA, Cochrane), highly preferred
• Experience in medical writing or demonstration in scientific writing ability in accordance with International Committee of Medical Journal Editors (ICMJE) authorship guidelines, preferred