Supervises clinical research studies from conception until completion. This field requires you to be on top of current laws and regulations that govern clinics and ensure that the clinic is operating incompliance with existing laws and regulations. Biotech Partners looks for candidates with experience preparing and tracking study timelines, managing budget and performance metrics, and making sure that good clinical practice (GCP)and regulatory compliance are maintained, negotiate contracts with clinical research organizations (CRO) and vendors and assist in the hiring and training of all clinical staff members. A CPM must be very well-rounded, as they are expected to manage all aspects of clinical research study. They must have exceptional written and verbal communication skills, as they will need to interact with a variety of professionals in the trial process.