Sr. Medical Writer (U.S. Remote & Temp to Hire)

Job Description INNOVATION STARTS WITH YOU 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 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 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. Qualifications • BA/BS degree • Three (3) to five (5) years of scientific experience. • Demonstrated experience in the development of regulatory/ clinical submissions (preferably as a medical writer for pharmaceutical, CRO, or medical device clients). • Excellent writing and editing skills, and 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 • The primary work location for this position is Tustin, CA (the company will be relocating to a new facility in Aliso Viejo, CA in Q3 2017). • 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 web site at www.microvention.com Apply tot his job Apply To this Job