Position Overview

This position will act as the primary contact for medical writing projects, cross-functionally working with MicroVention departments and clients to set and meet internal and external deliverables. Job duties:
  • Collaborate with the clinical team to write clinical documents for regulatory submissions, including but not limited to:
    • Clinical evaluation reports
    • Interim and final clinical study reports
    • Briefing documents
    • Previous human experience summaries
    • Investigator brochures
    • Study protocols
    • Medical literature analysis reports.
  • Research, create, and edit assigned clinical reports, documents and scientific presentations in cooperation with the Clinical, Medical, & Regulatory Affairs Teams, KOLs and physician investigators.
  • Conduct literature searches, manage the literature database and prepare literature reviews for external and internal clients.
  • Assist in the creation of clinical educational materials for the global Sales & Marketing organizations.
  • Perform additional responsibilities as assigned.
    1. Bachelor’s Degree in a related discipline.
    2. A minimum of three to five (3-5) years of scientific experience.
    3. Demonstrated experience in the development of regulatory/clinical submissions (preferably as a medical writer for medical devices, pharma or CRO).
    4. Excellent writing and editing skills, as well as attention to detail.
    Desired Qualifications
    1. Advanced degree (Ph.D, MD, Sc.D, MA/MS or MPH).
    2. Experience as an author or contributor or peer-reviewed manuscripts.
    3. Strong verbal, written, and interpersonal communication skills.
    4. Highly proficient in using MS Office applications (Word, Excel, PowerPoint) and Endnote.
    5. Expertise in conducting focused literature searches on PubMed, MedLine or other medical literature databases.