Principal Investigator Clinical Trials- Miami Job at EPM Scientific, Miami, FL

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  • EPM Scientific
  • Miami, FL

Job Description

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.

Job Tags

Monday to Friday, Weekend work, Weekday work

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