The PRN Sub Investigator (Sub I) plays a critical role in clinical research by supporting the Principal Investigator (PI) in the oversight and conduct of clinical trials. Depending on qualifications and site delegation, this role may also be eligible to be hired as either a Sub I or a PI.
The primary duty of the Sub I/PI is to protect human subjects and uphold their rights throughout the clinical trial. This role ensures that all delegated study activities are conducted in accordance with the protocol, Good Clinical Practice (GCP), and applicable federal regulations, while maintaining the integrity and validity of all data collected. This role is part time and estimated be 10-15 hours a week on site in Hollywood, FL. MUST be a MD and will be seeing patients.