Principal Investigator; MD​/DO Clinical Research – Cleveland, OH

Principal Investigator — Cleveland, OH

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.

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.

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.

• Serve as the Principal Investigator of record for assigned clinical trials (Phase II–IV; we do not conduct Phase I studies)
• 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

• MD, DO, or equivalent clinical degree with an active, unrestricted state medical license
• Experience as a Principal Investigator or Sub-Investigator on clinical trials (Phase II–IV experience preferred)
• 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

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.

Full-time or part-time, based on site and study needs.

The IMA Group is an affirmative action/Equal Opportunity Employer Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets.

Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.