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 Now
Apply Now
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 Now
Apply Now