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Principal Investigator; MD/DO Clinical Research – Philadelphia, PA
Job in
Philadelphia, Philadelphia County, Pennsylvania, 19102, USA
Listed on 2026-08-26
Listing for:
The IMA Group
Full Time, Part Time
position Listed on 2026-08-26
Job specializations:
-
Research/Development
Clinical Research
Job Description & How to Apply Below
Principal Investigator — Philadelphia, PA
IMA Clinical Research is expanding into Philadelphia and seeking a Principal Investigator for our newest clinical research site. This is an opportunity to support a new site launch while working within IMA's established research infrastructure, operational processes, and support model. Both full-time and part-time schedules may be considered.
What You'll Do
- Serve as the Principal Investigator of record for assigned clinical trials
- Conduct study-related medical evaluations and procedures in accordance with approved protocols
- Monitor participant safety throughout study participation
- Review protocols, informed consent materials, participant records, and relevant regulatory documentation
- Assess participant eligibility and review clinically significant findings
- Complete required study documentation accurately and within established timelines
- Communicate with sponsors, CROs, IRBs, and internal research teams as required
- Help establish relationships with local healthcare providers and community organizations
- Follow established IMA workflows, standard operating procedures, and regulatory requirements
What You Bring
- 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
- A collaborative approach and comfort working within an established, team-based research environment
Why Philadelphia
You'll have the opportunity to support the launch and growth of a new research site while benefiting from IMA's established workflows, experienced research teams, and clinical research infrastructure.
Schedule
Full-time or part-time, based on site and study needs.
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