Principal Investigator (MD/DO) – Clinical Research – Cleveland, OH

Posted One Month Ago
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Cleveland, OH, USA
In-Office
250K-325K Annually
Senior level
Professional Services • Design • Manufacturing
The Role
Serve as Principal Investigator for Phase II-IV clinical trials at a newly launched Cleveland research site. Responsibilities include conducting medical evaluations, monitoring participant safety, assessing eligibility, reviewing protocols and regulatory documentation, completing study records, and coordinating with sponsors, CROs, IRBs, and internal teams. The role also supports community relationship development and adherence to established research workflows and regulatory requirements.
Summary Generated by Built In

Principal Investigator — Cleveland, OH

IMA Clinical Research | New Site Launch

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.

We are seeking an experienced, entrepreneurial Principal Investigator with a strong track record in clinical trials who is excited to help establish and grow IMA Clinical Research in the Cleveland community.


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 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.

 

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

Skills Required

  • MD, DO, or equivalent clinical degree
  • Active, unrestricted state medical license
  • Experience as a Principal Investigator or Sub-Investigator on clinical trials
  • Phase II-IV clinical trial experience
  • Current GCP certification or willingness to obtain it before starting
  • Strong knowledge of ICH-GCP guidelines and FDA regulatory standards
  • Collaborative approach and comfort working in an established, team-based research environment
Am I A Good Fit?
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The Company
HQ: Tarrytown, NY
817 Employees
Year Founded: 1988

What We Do

The IMAGINE Group is a commercial printing company headquartered in Minneapolis, Minnesota. Its stated focus is providing communication solutions that put customers’ brands in the spotlight. The company maintains operations in the Twin Cities, Chicago, Charlotte, and Los Angeles, indicating a multi-location service footprint. Its core business is centered on producing print-based communications and supporting organizations’ branding and marketing needs through commercial print services.

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