Description
Intuitive is hiring a Clinical Evaluation Specialist to develop and maintain Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs) for medical devices under EU MDR. The role collaborates with engineering, product development, regulatory, and post-market surveillance teams; conducts literature searches and scientific appraisals; writes clinical documentation and regulatory responses; manages CEP/CER timelines; supports risk documentation and product labeling; and contributes to clinical study protocols and reports. Candidates need an MD, PhD, or M.S. in a scientific field, at least two years of medical writing experience, strong scientific writing and analytical skills, and experience with clinical evaluation and regulatory submissions.
