Principal Investigator (MD/DO) Clinical Research Louisville, KY

Principal Investigator Louisville, KY

IMA Clinical Research is expanding into Louisville, KY 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 Louisville, KY

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.