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Principal Investigator -Clinical Research (MD/DO) - PR/591114_1787865392

Principal Investigator -Clinical Research (MD/DO)

Tampa FL
Permanent
$350,000 - $400,000 USD a year
Clinical
PR/591114_1787865392
Principal Investigator -Clinical Research (MD/DO)

Principal Investigator Clinical Research (MD/DO) | Tampa, FL
$350,000-$400,000 Base + Bonus
Full-Time, On-Site
Relocation Assistance Available
Company
Our client is a well-established, multi-site clinical research organization with a growing footprint across the U.S., conducting industry-sponsored trials across a range of therapeutic areas including neurological, psychiatric, dermatologic, and specialty indications.
Position Summary
This is a full-time physician position focused exclusively on clinical research. We are seeking a Principal Investigator with prior clinical research/trial experience who will provide medical oversight across a portfolio of Phase I-IV industry-sponsored clinical trials while working closely with an experienced team of clinical research coordinators, regulatory professionals, and site leadership.
The incoming physician will step into active, well-supported research programs. This is not a ground-up build or a position where the physician is expected to create a research operation from scratch. You will inherit an established study pipeline, experienced research staff, and the support of a well-resourced site organization.
This is an opportunity for a physician to remain closely involved with patients and medical decision-making while building a long-term career at the forefront of clinical research.

Responsibilities

  • Serve as Principal Investigator for assigned industry-sponsored clinical trials
  • Evaluate prospective study participants and determine eligibility
  • Perform protocol-required medical assessments and oversee participant safety throughout each study
  • Review adverse events, laboratory results, medical histories, concomitant medications, and other relevant clinical information
  • Ensure trials are conducted in accordance with study protocols, ICH-GCP guidelines, FDA regulations, and applicable requirements
  • Review and sign source documentation, study records, safety reports, and other required materials
  • Provide medical guidance to clinical research coordinators and other members of the site team
  • Collaborate with sponsors, CROs, medical monitors, and regulatory representatives
  • Support patient enrollment, protocol compliance, data quality, and successful study execution

Qualifications

  • MD or DO degree
  • Board-certified US licensed Physician
  • Previous clinical research experience as a Principal Investigator, Sub-Investigator, research physician, or in a comparable capacity
  • Active Florida medical license or eligibility to obtain one
  • DEA registration or ability to obtain one
  • Working knowledge of ICH-GCP guidelines and clinical research regulations
  • Strong clinical judgment and commitment to participant safety
Previous experience serving as a Principal Investigator on industry-sponsored trials is preferred. Physicians with meaningful Sub-Investigator or clinical trial experience who are prepared to step into a full-time Principal Investigator position are also encouraged to apply.

Compensation & Benefits:

This full-time position offers a $350,000-$400,000 base salary + bonus, based on experience, along with a comprehensive benefits package that includes medical, dental, and vision insurance, a 401(k) retirement plan, paid time off, company holidays, and additional employer-sponsored benefits. Relocation assistance is available for qualified candidates.

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