A leading clinical research organization is seeking an experienced Regulatory Affairs Consultant to join their team in Uxbridge. This mid-senior level role focuses on in-vitro diagnostics and companion diagnostics, requiring expertise in regulatory pathways and strong collaboration with cross-functional teams. Ideal candidates have over 5 years of experience in medical device regulatory affairs and possess a scientific degree. The position offers a full-time contract in a dynamic environment. #J-18808-Ljbffr