Principal Investigator l Part-Time l Orlando & Tampa l Multiple Specialties - 24

As a Principal Investigator, you will provide medical oversight and leadership for clinical trials. You will be responsible for ensuring subject safety, regulatory compliance, and protocol adherence throughout the duration of the study. The site team will support you with daily operations, allowing you to focus on medical decision-making and oversight. Specialty Breakdowns by City:

Orlando, FL Internal Medicine (Greatest Need) Neurology Psychiatry Dermatology Cardiology Endocrinology Hepatology Gastroenterology

Tampa, FL Internal Medicine (Greatest Need) Neurology Psychiatry Dermatology Cardiology Endocrinology Hepatology Gastroenterology Schedule: Flexible with days, but seeking a minimum of 2 days/week of availability (8 hours days). It's Phases 2-4 so no weekend or on call work. M-F, 8-5 availability needed. Compensation: There is a training and post-training rate. Compensation is based on specialty, availability and location. Key Responsibilities: Serve as Principal Investigator on assigned clinical trials Conduct and/or oversee study-related assessments, including subject eligibility, informed consent and safety evaluations Ensure compliance with study protocols, GCP, FDA regulations, and IRB requirements Collaborate with study sponsors, CROs, and internal staff throughout the trial lifecycle Review and sign off on case report forms (CRFs), adverse events, and safety data Participate in Site Initiation Visits, Monitoring Visits, Investigator Meetings and other Sponsor meetings as needed Provide guidance and medical support to the research team