Position Overview


Are you interested in working for an organization that is making a difference in people’s lives every day? We’re a medical devices company that develops innovative neuroendovascular technologies for the treatment of vascular disease. We’re a high-growth, customer-focused company with an entrepreneurial spirit producing some of the most reliable and technologically advanced products supported by proven clinical data. Take a closer look at what MicroVention® TERUMO has to offer.

Position Overview

The Sr. Medical Writer/Medical Writerwill act as primary contact for medical writing projects, cross-functionally working with MicroVention departments and clients to set and meet internal and external deliverables. Some typical job duties include:
  • Collaborating with the clinical & regulatory teams 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.
  • Conducting literature searches, manage the literature database, and prepare literature reviews for external and internal clients.
  • Assisting in the creation of clinical educational materials for the global Sales & Marketing organizations.
  • ​​​​Medical Writer Qualifications
    • BA/BS degree
    • Three (3) to five (5) years of scientific experience.
    • Demonstrated experience in the development ofregulatory/ clinical submissions (preferably as a medical writer for pharmaceutical, CRO, or medical device clients).
    • Excellent writing and editing skills, and attention to detail.

    ​​​​Sr. Medical Writer Qualifications
    • Bachelor’s Degree in a related discipline.
    • At least six (6) years of scientific experience.
    • Demonstrated experience in the development of regulatory/clinical submissions (preferably as a medical writer for medical devices, pharma or CRO).
    • Excellent writing and editing skills, as well as attention to detail.

    Desired Qualifications
    • Advanced degree (Ph.D, MD, Sc.D, MA/MS or MPH).Experience as author or contributor of peer-reviewed manuscripts is strongly desired.
    • Strong verbal, written, and interpersonal communication skills.
    • Highly proficient in using Microsoft Office applications (Word, Excel, PowerPoint) and EndNote.
    • Expertise in conducting focused literature searches on PubMed, MedLine or other similar medical literature databases.
    Additional Information
    • Relocation may be available for qualified candidates.
    • Candidates must be eligible to work in the U.S. and not require visa sponsorship.
    • For more information, visit our website atwww.microvention.com