Knowledge of research protocols, principles, and procedures related to clinical trialssuch as screening, interviewing, and case report forms; basic knowledge of experimental design, computerized information retrieval systems, and computer data management; ability to identify, produce, organize data; knowledge of or ability to learn ethics and regulatory procedures (e.g., informed consent process, data safety, and monitoring plans, principles of data collection and documentation) involved with clinical research; ability to work as a member of a project team. JOB SUMMARY: The Clinical Research Coordinator, under the guidance and supervision of the Principal Investigator (PI) and the Clinical Research Nurse Coordinator, supports the integrity and quality of human subjects research (clinical trials), maintained and conducted in accordance with federal, state, and local regulations, Institutional Review Board (IRB) approvals, and MAHEC policies and procedures.