Clinical Research Sub-Investigator (PA or NP)

Conduct study-related clinical evaluations, including medical histories, physical examinations, and protocol-required assessments under the supervision of the Principal Investigator. Assess and document adverse events, serious adverse events, and protocol deviations in accordance with study protocols and regulatory requirements. Ensure participant safety and protocol compliance during study visits while collaborating with the clinical research coordination team to support participant recruitment, eligibility determination, and completion of study visits. Communicate with study sponsors and contract research organizations regarding protocol execution, participant status, safety reporting, and study-related questions. Participate in study-related meetings, monitoring visits, and investigator meetings when required. Maintain compliance with Good Clinical Practice (GCP), institutional policies, and regulatory standards. Standard working hours are Monday–Friday, 8:00 AM – 5:00 PM.