Remote Clinical Evaluation Reports Medical Writer - Midland
Check out similar listings!
Loading some great jobs for you...
A communication solutions provider is filling a position for a Remote Clinical Evaluation Reports Medical Writer. Core Responsibilities Include: Evaluating data for similar competitor devices Screening and summarizing literature for relevant clinical data Ensuring timely production of high quality CERs for devices across therapeutic areas Must meet the following requirements for consideration: Willingness to travel to India office up to 2 times a year Experience across document types and therapeutic areas/diseases/drug classes 1-2 years of regulatory writing experience, with some exposure to medical devices A MD, PhD in Biomedical Engineering or similar degree, a Master's degree with clinical research exposure can also be considered 5+ years of CER writing experience in a medical device company, CRO, or agency Advanced knowledge of 510(k), MedDEV 2.7.1 Rev 4, MDR, and other relevant medical device regulations Associated topics: aseptic, diet, dietetic, drug discovery, food scientist, healthcare, kinesiology, medicine, microbiological, pharmacy
* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.