Sr. Medical Writer; U.S. Remote & Temp

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 Micro Vention
® TERUMO has to offer. The Sr. Medical Writer/Medical Writer will act as primary contact for medical writing projects, cross-functionally working with Micro Vention 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.

$111,000 - $145,000 Financial compensation packages may be higher/lower than what is listed, & will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand.

Job  

• 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 device clients).
• Excellent writing and editing skills, and attention to detail.
• 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 End Note.
• Expertise in conducting focused literature searches on Pub Med, Med Line or other similar medical literature databases.
• 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.

We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, veteran status, marital status or any other characteristics protected by law. If you are applying to perform work for Terumo Neuro in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Terumo Neuro reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

Terumo Neuro will consider for employment qualified job applicants with arrest or conviction records in accordance with the California Fair Chance Act, Los Angeles County Fair Chance Ordinance for Employers, Fair Chance Initiative for Hiring Ordinance, and San Francisco Fair Chance Ordinance.