We are looking for several experienced Clinical Evaluation Report Writers to join a group of expanding medical device companies. Responsibilities include:
Writing and contributing to Clinical Evaluation Reports and Plans, Post Market Clinical Follow-up Plans and Reports, and Summaries of Safety and Clinical Performance.
Conducting literature reviews
Report and protocol generation
Writing PMS Plans and Reports
Updating instructions for use and risk assessments following clinical review
Undertaking biological evaluations
Sourcing BER data
Successful candidates will have a relevant scientific or engineering degree and experience writing CER’s complying to current medical device standards. They will also have excellent communication skills.
PLEASE NOTE THAT CANDIDATES ARE REQUIRED TO BE BASED IN THE UK AND HAVE THE RIGHT TO WORK IN THE UK