What are the responsibilities and job description for the Principal Investigator Clinical Trials- Miami position at EPM Scientific?
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.