Terumo Group
Sr. Medical Writer (U.S. Remote & Temp to Hire)
Terumo Group, California, Missouri, United States, 65018
Sr. Medical Writer (U.S. Remote & Temp to Hire)
Position Overview
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 the primary contact for medical writing projects, working cross-functionally with MicroVention departments and clients to set and meet internal and external deliverables. Typical duties include: Collaborating with 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 clinical reports, documents, and scientific presentations in cooperation with Clinical, Medical, & Regulatory Affairs Teams, KOLs, and physician investigators. Conduct literature searches, manage literature databases, and prepare literature reviews for internal and external clients. Assist in creating clinical educational materials for global Sales & Marketing organizations. Job ID 12933BR Salary Range: $111,000 - $145,000 (compensation may be higher based on education, experience, and skills) Three to five years of scientific experience. Experience in developing regulatory/clinical submissions, preferably as a medical writer for pharmaceutical, CRO, or medical device clients. Excellent writing, editing skills, and attention to detail. BA/BS degree Advanced degree (Ph.D., MD, Sc.D., MA/MS, or MPH). Peer-reviewed manuscript experience is strongly desired. Strong verbal, written, and interpersonal communication skills. Proficient in Microsoft Office applications (Word, Excel, PowerPoint) and EndNote. Experienced in conducting focused literature searches on PubMed, MedLine, or similar databases. The primary work location is Tustin, CA, with relocation to 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.
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Position Overview
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 the primary contact for medical writing projects, working cross-functionally with MicroVention departments and clients to set and meet internal and external deliverables. Typical duties include: Collaborating with 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 clinical reports, documents, and scientific presentations in cooperation with Clinical, Medical, & Regulatory Affairs Teams, KOLs, and physician investigators. Conduct literature searches, manage literature databases, and prepare literature reviews for internal and external clients. Assist in creating clinical educational materials for global Sales & Marketing organizations. Job ID 12933BR Salary Range: $111,000 - $145,000 (compensation may be higher based on education, experience, and skills) Three to five years of scientific experience. Experience in developing regulatory/clinical submissions, preferably as a medical writer for pharmaceutical, CRO, or medical device clients. Excellent writing, editing skills, and attention to detail. BA/BS degree Advanced degree (Ph.D., MD, Sc.D., MA/MS, or MPH). Peer-reviewed manuscript experience is strongly desired. Strong verbal, written, and interpersonal communication skills. Proficient in Microsoft Office applications (Word, Excel, PowerPoint) and EndNote. Experienced in conducting focused literature searches on PubMed, MedLine, or similar databases. The primary work location is Tustin, CA, with relocation to 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.
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