Experience with recruitment, informed consent, source documentation, EDC entry, query resolution, IRB submissions, monitoring visits, investigational-product accountability, specimen processing or shipping, and study closeout; ACRP or SoCRA certification; Experience with remote participant follow-up, electronic consent, wearable or connected devices, or other technology-enabled study activities; Experience performing phlebotomy, vital signs, EKG acquisition, laboratory specimen processing, or other protocol-required procedures; Current, unrestricted RN license or another relevant clinical credential, with experience applicable to the assigned research activities; Experience in diabetes, endocrinology, primary care, behavioral health, or another therapeutic area relevant to MAHEC’s research portfolio. Knowledge of research protocols, principles, and procedures related to clinical trials such 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.