Principal Investigator (MD/DO) – Clinical Research – Cleveland, OH
About the role
IMA Clinical Research is expanding into Cleveland, OH 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.
Compensation
This role offers competitive compensation of $250,000–$325,000 on a full-time basis, based on clinical research experience, therapeutic expertise, and demonstrated success as a Principal Investigator. Additional earning potential is available through a revenue-sharing incentive tied to the site’s growth and performance.
Responsibilities
- 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
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
- A collaborative approach and comfort working within an established, team-based research environment
About Cleveland, OH
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.