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Clinical Trials Part Time Jobs in Ohio (NOW HIRING)

IQVIA

Clinical Trial Psych Rater

Cleveland, OH · Remote

$62K - $156K/yr

Experience in CNS trials preferred. * Skills: * Strong interpersonal and communication skills for ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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Clinical Trials Part Time information

What is a clinical trials part time job?

Clinical trials part time jobs are positions in which individuals assist with the planning, execution, or management of clinical research studies on a part-time basis. These roles may include research assistants, coordinators, data managers, or nurses, and offer flexible work hours to accommodate other commitments. Part-time staff are crucial in supporting the collection and management of data, participant recruitment, and ensuring compliance with study protocols. These positions are ideal for students, professionals seeking flexible hours, or those looking to gain experience in clinical research without committing to a full-time schedule.

What are the common responsibilities and challenges of working part-time in clinical trials?

Part-time roles in clinical trials typically involve supporting research coordinators, assisting with data collection and entry, participant recruitment, and ensuring compliance with study protocols. A common challenge can be balancing workload and communication with the team, as studies often require careful coordination and timely updates. Flexibility and strong organizational skills are important, as part-time staff may need to quickly adapt to changing priorities while maintaining high-quality standards. Despite these challenges, part-time positions offer valuable exposure to clinical research processes and can serve as a stepping stone to full-time roles or advanced positions in the field.

What are the key skills and qualifications needed to thrive in a part-time clinical trials role, and why are they important?

To thrive in a part-time clinical trials role, you typically need a background in life sciences or healthcare, attention to detail, and familiarity with clinical research protocols. Experience with electronic data capture (EDC) systems, knowledge of Good Clinical Practice (GCP), and sometimes certification such as SOCRA or ACRP are commonly required. Strong organizational skills, clear communication, and adaptability help you excel in coordinating studies and working with diverse teams. These skills ensure accurate data collection, regulatory compliance, and efficient support of clinical research objectives.

What is the difference between Clinical Trials Part Time vs Clinical Research Coordinator?

AspectClinical Trials Part TimeClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field; certifications like CCRP are a plusRequires a degree in health sciences or related field; often holds certifications such as CCRP or CCRC
Work EnvironmentPart-time roles in clinics, hospitals, or research facilities; flexible schedulesFull-time or part-time roles in research sites, hospitals, or pharmaceutical companies
Employer & IndustryPharmaceutical companies, CROs, academic institutionsResearch sites, hospitals, pharmaceutical companies

Clinical Trials Part Time roles focus on supporting specific trial activities with flexible hours, while Clinical Research Coordinators oversee entire study processes, often working full-time. Both roles require similar credentials and are integral to clinical research, but differ mainly in scope and schedule.

What are the most commonly searched types of Clinical Trials jobs in Ohio?

The most popular types of Clinical Trials jobs in Ohio are:

What cities in Ohio are hiring for Clinical Trials Part Time jobs?

Cities in Ohio with the most Clinical Trials Part Time job openings:

Clinical Trials Part Time jobs near you
Infographic showing various Clinical Trials Part Time job openings in Ohio as of August 2026, with employment types broken down into 3% As Needed, 76% Full Time, 14% Part Time, and 7% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

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

Cleveland, OH

The IMA Group
Health Care and Social Assistance • 201 - 500 employees
Learn more about The IMA Groupexternal

Full-time, Part-time

Posted 5 days ago

Job description

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. 
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About IMA Group

Sourced by ZipRecruiter

IMA Group is a prominent player in the healthcare sector headquartered in Tarrytown, NY, USA. The company is known for offering a range of comprehensive health assessments, disability evaluations, as well as related services. It has been providing these services for over three decades, having been established back in the late 1980s. IMA Group is driven by a core mission – to assist individuals and families through challenging times of their lives with their health and disability-related services. The company believes in delivering personalized, professional, and compassionate service.

Industry

Health care and social assistance

Company size

201 - 500 Employees

Headquarters location

Tarrytown, NY, US

Year founded

1990

Social media

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