Lead PI, Clinical Trials (Phase II–IV) – Philadelphia

The IMA Group; Philadelphia (Philadelphia County); On-site; USD 150,000 - 210,000; Full time

Benefits offered by this job

Equal Opportunity Employer

Job summary

The IMA Group is launching a new clinical research site in Philadelphia. We are seeking a Principal Investigator to lead Phase II–IV trials within our established research framework and support model.

Ideal candidates hold an active medical license (MD/DO or equivalent) and have PI or Sub-PI experience. GCP certification is required or obtainable before start. Flexible scheduling may apply for full-time or part-time appointments.

Qualifications

• MD/DO or equivalent clinical degree and active, unrestricted state medical license.
• Experience as PI or Sub-Investigator on Phase II–IV trials (Phase I not conducted).
• Current GCP certification or willingness to obtain prior to starting.

Responsibilities

• Serve as the Principal Investigator of record for assigned clinical trials (Phase II–IV).
• Conduct study-related medical evaluations and procedures per approved protocols.
• Monitor participant safety throughout study participation.
• Review protocols, informed consent materials, records, and regulatory documents.
• Assess participant eligibility and review clinically significant findings.
• Complete required study documentation accurately and timely.
• Communicate with sponsors, CROs, IRBs, and internal teams as required.
• Establish relationships with local healthcare providers and community organizations.
• Follow IMA workflows, SOPs, and regulatory requirements.

Skills

ICH-GCP knowledge

FDA regulatory standards

Collaborative approach

Education

MD/DO or equivalent clinical degree

Tools

GCP certification

Job description

The IMA Group is launching a new clinical research site in Philadelphia. We are seeking a Principal Investigator to lead Phase II–IV trials within our established research framework and support model.

Ideal candidates hold an active medical license (MD/DO or equivalent) and have PI or Sub-PI experience. GCP certification is required or obtainable before start. Flexible scheduling may apply for full-time or part-time appointments.