Principal Investigator Clinical Trials- Miami
Principal Investigator (Internal Medicine or Family Medicine) - 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 [insert range here] + benefits (medical, dental, vision).
- 401(k) with match; paid time off and holidays.
- Ongoing professional development and research training.
FAQs
Congratulations, we understand that taking the time to apply is a big step. When you apply, your details go directly to the consultant who is sourcing talent. Due to demand, we may not get back to all applicants that have applied. However, we always keep your resume and details on file so when we see similar roles or see skillsets that drive growth in organizations, we will always reach out to discuss opportunities.
Yes. Even if this role isn’t a perfect match, applying allows us to understand your expertise and ambitions, ensuring you're on our radar for the right opportunity when it arises.
We also work in several ways, firstly we advertise our roles available on our site, however, often due to confidentiality we may not post all. We also work with clients who are more focused on skills and understanding what is required to future-proof their business.
That's why we recommend registering your resume so you can be considered for roles that have yet to be created.
Yes, we help with CV and interview preparation. From customized support on how to optimize your CV to interview preparation and compensation negotiations, we advocate for you throughout your next career move.