Physician (Part-Time)

Position Objective The Physician will independently provide support services to satisfy the overall operational objectives of the National Institute of Mental Health (NIMH) within the National Institutes of Health (NIH). Duties and Responsibilities Provide analyses, evaluations, technical assessments, feedback and support in the planning and implementation of activities. Administer and monitor clinical and basic research projects, including clinical trials, ensuring protection and safety of participants. Provide expertise during ongoing trials, such as suitability of volunteers for enrollment, consultation for protocol PIs, and safety oversight/assessments. Review clinical protocols for safety, provide medical expertise in protocol follow‑up stages, and assess serious adverse events (SAEs). Review safety reports, represent the Program as a safety expert on safety committees, and evaluate reporting strategies and safety monitoring plans. Participate in clinical trial Steering Committee decisions on selection and implementation of interventions, review clinical outcomes, and assure participant safety. Produce detailed reports for upper clinic or laboratory management based on safety monitoring plans and study progress. Coordinate all aspects of clinical protocol development, review, and implementation; advise program management on merits and deficiencies of proposed studies. Provide advice on oversight of clinical trials and protocols, including IRB processes and clinical patient care. Assist in developing protocols for future clinical projects and Investigational New Drug (IND) applications. Identify process and implementation gaps, manage escalation, and participate in resolution. Ensure funded research is scientifically valid and complies with Institute/Center, NIH and DHHS priorities; monitor post‑award administration. Write policies and guidelines on safety‑related issues. Attend and participate in scientific meetings, conferences, and training programs; serve as a medical liaison between the institute and research working groups. Maintain patient and protocol records and provide status updates of ongoing projects. Basic Qualifications M.D. required Licensed physician or board eligible Skilled in clinical research, medical training, patient care, risk management, and site visits. Skilled in regulatory, human research subject protections, subject recruitment/enrollment, and clinical protocol review Experience in administrative summaries, clinical trial oversight, and subject matter expert Experience with CRIS, CTDB, MS Office Suite, Outlook Preferred Qualifications Strong communication skills, both oral and written Detail‑oriented and possess strong organizational skills with the ability to prioritize multiple tasks and projects Additional Information *This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required by this position. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Equal Opportunity / EEO Statement Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by law. #J-18808-Ljbffr GAP Solutions Inc