Clinical Research Coordinator: Patient-Focused Trials

Job Description Job Description Summary: The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, Optimed Research, Sponsor, and CRO to support and provide guidance on all aspects of the clinical study. Responsibilities: 1. Serves as the main point of contact for all patients participating in the clinical research study. 2. Manages all aspects of patient visits during the course of a study. 3. Ensures clinical processes follow the study protocol. 4. Examines medical history to assess patients’ eligibility for participation in the research study. 5. Facilitates the informed consent process with the patient and family. 6. Collects and enters data into the e-source system. 7. Prepares lab kits for research visits. 8. Performs blood draws and processes blood and samples for shipping. The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this position. It is not to be construed as an exhaustive list of duties performed by the individual so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under his/her supervision. #J-18808-Ljbffr