Principal Investigator
The IMA Group • Cleveland, OH78d • Onsite
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Principal Investigator (MD/DO) – Clinical Research – Philadelphia, PA
The IMA Group•Cleveland, OH
•Onsite
About The Position
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. 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.
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
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
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What This Job Offers
Job Type
Full-time
Career Level
Principal
Education Level
Ph.D. or professional degree
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