Endocrinology Physician

Oversee and conduct clinical research protocols in accordance with GCP and regulatory requirements. Perform medical assessments and provide clinical oversight for study participants. Collaborate with research staff to ensure data integrity and protocol compliance . Review and sign off on source documents, adverse event reports, and case report forms. Maintain regular communication with study sponsors and CRO. Qualifications: Active medical license in North Carolina, Board certification in any specialty (internal medicine, family medicine, psychiatry, etc. preferred),Prior clinical research experience a plus, but not required, Strong attention to detail, organizational skills, and commitment to protocol adherence, Excellent communication and collaborative abilities. Schedule: 8 hours per week, on-site (1 day/week); remaining tasks may be completed remotely/hybrid