This is a Temp-To-Hire Position The Sr. Medical Writer/Medical Writer will act as primary contact for medical writing projects, cross-functionally working with Terumo Neuro 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.