Principal Investigator - Family/Internal Medicine
$208,000–$208,000 year
On-site · Omaha, Nebraska, United States
Job Summary
Principal Investigator responsible for overall conduct, oversight, and integrity of clinical trials at the site. Provides medical and scientific leadership, ensures subject safety, regulatory compliance (ICH-GCP, FDA regulations, IRB/IBC, sponsor protocols), supervision of delegated staff, and accountability for trial-related activities. Oversees regulatory and QA activities, protocol execution, enrollment strategy, and ethical recruitment; ensures data integrity (ALCOA-C) and audit-ready documentation; collaborates with Clinical Operations, Compliance, Regulatory, Quality Control, and Recruitment teams. Requires MD or DO with active license, current GCP certification, and DEA license if required by study protocol. Location: Omaha, NE (contractor role).
Required Qualifications
- MD or DO with active, unrestricted medical license in applicable state
- Current GCP certification (or ability to obtain upon onboarding)
- DEA license (if required by study protocol)
- Prior experience as a Principal Investigator strongly preferred
- Demonstrated knowledge of ICH-GCP guidelines, FDA regulations, clinical trial processes
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