Principal Investigator Clinical Trials- Miami (Miami)

Principal Investigator Clinical Trials - Miami, FL

Onsite (Monday-Friday)

Clinical Research Site

Role Summary

Join a high‑performing clinical research site and lead Phase I-IV studies as the Principal Investigator (PI) in Miami. You'll provide medical oversight, protect participant safety, and ensure protocol and regulatory compliance while collaborating with an experienced research team.

Non‑negotiable: Board‑Certified Internal Medicine or Family Medicine physician, active Florida MD license , and onsite in Miami, Monday-Friday .

What You'll Do (top responsibilities)

• Lead assigned clinical trials as PI; make trial‑related medical decisions and provide day‑to‑day oversight.
• Perform physical exams, medical assessments, and ongoing safety evaluations.
• Determine eligibility per inclusion/exclusion criteria; document decisions clearly.
• Monitor response to investigational products; assess and manage adverse events per protocol.
• Ensure GCP/ICH, FDA, IRB, and SOP compliance; maintain audit‑ready documentation.
• Partner with site leadership and coordinators on enrollment plans and visit execution.
• Mentor Sub‑Investigators and guide clinical staff on protocol fidelity and patient safety.

Must‑Have Qualifications

• Board Certification: Internal Medicine or Family Medicine (MD).
• License: Active, unrestricted Florida medical license.
• Availability: Onsite in Miami , Monday-Friday (not remote/hybrid).
• Demonstrated clinical judgment, clear documentation, and strong patient‑safety focus.
• Professional communication and teamwork in a regulated, protocol‑driven setting.

Preferred (nice to have)

• Prior experience as PI or Sub‑Investigator .
• Working knowledge of GCP/ICH , IRB processes, and monitoring/audit readiness.
• Experience with structured assessments or research‑based evaluations.
• EMR proficiency and familiarity with standard clinical research platforms.

Schedule & Work Environment

• Dedicated onsite research facility; daytime weekday schedule.
• Collaborative team (CRCs, Sub‑Is, regulatory staff) focused on quality and compliance.
• No nights, weekends, or on‑call.

Compensation & Benefits

• Competitive base compensation + benefits (medical, dental, vision).
• 401(k) with match; paid time off and holidays.
• Ongoing professional development and research training.