Role OverviewWe are seeking a Principal Investigator to support the launch and growth of a new research site in Philadelphia. The successful candidate will work within IMA's established research infrastructure, operational processes, and support model. This is an opportunity to work in a team-based research environment and support the launch of a new site.
What You Will Do
The Principal Investigator will serve as the Investigator of record for assigned clinical trials, conduct study-related medical evaluations and procedures, and monitor participant safety. They will also review protocols, informed consent materials, and participant records, and communicate with sponsors, CROs, IRBs, and internal research teams.
Why It Might Be a Fit
The ideal candidate will have a collaborative approach, a 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
- Strong knowledge of ICH-GCP guidelines and FDA regulatory standards
Benefits
- Flexible part-time or full-time schedule
- Opportunity to support the launch and growth of a new research site
- Established research infrastructure and support model
- Collaborative team-based research environment
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