Sr. Medical Writer

The Sr. Medical Writer/Medical Writer will 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 reportsInterim and final clinical study reportsBriefing documentsPrevious human experience summariesInvestigator brochuresStudy protocolsMedical 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.