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Principal Investigator (MD/DO) – Clinical Research – Augusta, GA

The IMA Group
Posted 15 days ago, valid for 19 days
Location

Augusta, GA, US

Salary

Competitive

Contract type

Part Time

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Sonic Summary

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  • IMA Clinical Research is seeking a Principal Investigator for a new clinical research site in Augusta, GA, with both full-time and part-time schedules available.
  • The role requires an MD, DO, or equivalent clinical degree with an active and unrestricted state medical license, along with experience as a Principal Investigator or Sub-Investigator on clinical trials, specifically Phase II–IV.
  • Candidates must possess current GCP certification or be willing to obtain it before starting, and have strong knowledge of ICH-GCP guidelines and FDA regulatory standards.
  • The Principal Investigator will be responsible for conducting medical evaluations, monitoring participant safety, and ensuring compliance with protocols and regulatory requirements.
  • Salary details are not specified in the job listing, but experience in clinical trials is required to qualify for this position.

Principal Investigator — Augusta, GA

IMA Clinical Research | New Site Launch

IMA Clinical Research is expanding into Augusta, GA 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 (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

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 (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

Why Augusta, GA?
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.

 

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.  
 

#LI-RC1 #LI-ONSITE




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