Clinical Evaluation Report Writer

The role

You'll author and update Clinical Evaluation Reports (CERs) and Clinical Evaluation Plans (CEPs) for medical device manufacturers submitting to international regulatory bodies. Working remotely with life science consultants, regulatory affairs directors, and medical reviewers, you'll analyze clinical trial data, literature searches, and post-market safety records under EU MDR standards. It requires a bachelor's degree in science or medicine and 1 to 5 years of medical device regulatory writing experience.

Tools and skills