Role OverviewWe are seeking an experienced Principal Investigator to support the launch and growth of a new research site in Cleveland, OH. The Principal Investigator will serve as the lead investigator for assigned clinical trials, conduct medical evaluations, and monitor participant safety. The role offers competitive compensation and a revenue-sharing incentive tied to the site's growth and performance.
What You Will Do
The Principal Investigator will conduct study-related medical evaluations, monitor participant safety, review protocols and informed consent materials, and communicate with sponsors, CROs, and internal research teams.
Why It Might Be a Fit
The ideal candidate will have a strong track record in clinical trials, a collaborative approach, and comfort working within an established research environment. The Principal Investigator will have the opportunity to support the launch and growth of a new research site while benefiting from IMA's established workflows and research infrastructure.
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
- Strong knowledge of ICH-GCP guidelines and FDA regulatory standards
Benefits
- Competitive compensation of $250,000–$325,000 on a full-time basis
- Revenue-sharing incentive tied to the site's growth and performance
- Opportunity to support the launch and growth of a new research site
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