
Medical Writer
Primarily responsible for writing and maintaining Clinical Evaluation Reports and Post Market Surveillance Reports for all the CSH portfolio of products. Collaborate (writing, reviewing, editing and approval) with clinical, R&D, quality assurance, regulatory and marketing teams on clinical study reports, clinical evidence gap assessments, marketing brochures, post-market surveillance reports, risk management documents and other documents that require the evaluation of clinical data and/or clinical literature. Create and manage project schedules for each clinical evidence document. Administration of the applicable databases for the activities related to the evaluation of clinical data, Clinical Evaluation reports and Post Market surveillance reporting.
Minimum of 4 years of clinical experience
Knowledge of extracorporeal devices, surgical and transcatheter heart valves, or coronary and renal denervation devices is desired
Direct experience with medical and/or scientific writing within a medical device industry or related industry
Familiarity with current regulatory agency guidances and regulations, including EU MDR and MEDDEV Rev 4
Medtronic product experience strongly preferred
Database Management
Report Writing
Scientific writing
Endnote Libraries
Quosa
Process Improvement
Verbal communication
Detail Oriented
written communication
Results driven
According to JobzMall, the average salary range for a Medical Writer in 3576 Unocal Pl, Santa Rosa, CA 95403, USA is $66,000 to $92,000. This range can be affected by various factors, such as the type of company, the experience of the medical writer, and the location of the job.
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Medtronic plc is the world's largest medical device company that generates the majority of its sales and profits from the US healthcare system and is headquartered on the island of Ireland.

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