Role OverviewWe are seeking a Principal Investigator to support the launch and growth of a new research site in Louisville, KY. The successful candidate will work within IMA's established research infrastructure, operational processes, and support model. This is an opportunity to support a new site launch while working within a team-based research environment.
What You Will Do
The Principal Investigator will serve as the Principal Investigator of record for assigned clinical trials, conduct study-related medical evaluations and procedures, monitor participant safety, and communicate with sponsors, CROs, IRBs, and internal research teams.
Why It Might Be a Fit
The ideal candidate will have a collaborative approach, strong knowledge of ICH-GCP guidelines and FDA regulatory standards, and experience as a Principal Investigator or Sub-Investigator on clinical trials.
Requirements
- MD, DO, or equivalent clinical degree with an active, unrestricted state medical license
- Experience as a Principal Investigator or Sub-Investigator on clinical trials
- Current GCP certification or willingness to obtain it before starting
Benefits
- Part-time or full-time schedule
- Opportunity to support a new site launch
- Established research infrastructure and support model
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