Description
The Sub-Investigator serves as the secondary physician responsible for medical and clinical oversight at a clinical research site, acting in place of the Principal Investigator when needed. The role supports protocol compliance, subject recruitment and care, informed consent, adverse-event reporting, data accuracy, investigational-product handling, regulatory and IRB requirements, monitoring and audit participation, and site operations. It requires Nurse Practitioner qualification, current licensure, and experience in industry-sponsored clinical trials, with preferred Sub-Investigator experience.
