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Part Time Clinical Research Contract Jobs (NOW HIRING)

The Pennsylvania State University

$23.75 - $31.75/hr

Kristina Petersen's labin the Department of Nutritional Sciences is seekinga part-time Clinical Research Coordinator to support externally funded clinical trials investigating dietary interventions ...

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Part Time Clinical Research Contract information

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How much do part time clinical research contract jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for part time clinical research contract in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

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

AspectPart Time Clinical Research ContractPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree in health sciences or related field; often holds certifications like CCRP or CRC
Work EnvironmentTemporary, project-based settings within research organizations or pharmaceutical companiesOngoing role within clinical sites or research organizations, overseeing study activities
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for specific projectsCommonly employed by hospitals, research centers, and clinical trial sites

In summary, a Part Time Clinical Research Contract is a temporary, project-specific role often filled by professionals with relevant certifications, while a Part Time Clinical Research Coordinator is a more ongoing position responsible for managing daily study activities at clinical sites. Both roles require similar credentials but differ in scope and employment type.

What are some typical responsibilities and challenges faced in a part-time clinical research contract role?

In a part-time clinical research contract role, you may be responsible for tasks such as data collection, patient recruitment, regulatory documentation, and coordinating study visits, often within a limited number of hours each week. One common challenge is balancing multiple studies or priorities while adhering to strict compliance and reporting deadlines. You’ll frequently collaborate with research coordinators, principal investigators, and sometimes sponsors to ensure the smooth progress of clinical trials. Adapting quickly to evolving protocols and maintaining clear communication with the team are key to success in this flexible, yet demanding, position.

What is a part-time clinical research contract?

A part-time clinical research contract is a work agreement where an individual is hired to assist with clinical research projects on a part-time basis, typically for a set duration or specific project. These contracts often involve roles such as study coordination, data collection, patient recruitment, or regulatory compliance. The part-time nature allows flexibility in hours and workload, making it ideal for students or professionals seeking supplementary experience. Contract terms, responsibilities, and compensation are usually outlined clearly before work begins. This arrangement benefits both employers needing temporary or specialized help and workers seeking flexible opportunities.

What are the key skills and qualifications needed to thrive as a Part Time Clinical Research Contract professional, and why are they important?

To thrive in a Part Time Clinical Research Contract role, you need a solid understanding of clinical research processes, regulatory compliance, and relevant science or healthcare education. Familiarity with tools such as clinical trial management systems (CTMS), electronic data capture (EDC), and knowledge of GCP (Good Clinical Practice) guidelines or related certifications is often required. Strong organizational skills, attention to detail, and effective communication are critical soft skills for coordinating studies and liaising with stakeholders. These competencies ensure protocol adherence, data integrity, and successful collaboration within research teams.
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Part Time Clinical Research Contract jobs near you
Part-Time Clinical Research gastroenterologist

Part-Time Clinical Research gastroenterologist

ProTouch Staffing

Asheville, NC

$100 - $250/hr

Part-time

Posted 11 days ago

Job description

Job Title:  Part-Time Clinical Research gastroenterologist

Compensation: $100 - $250 per hour
Schedule: Part-Time (0-8 hours)
start date: 0-6 months

About the Role

We are seeking a board-certified to serve as a Clinical Research gastroenterologist

You will oversee protocol compliance, ensure patient safety, and collaborate with sponsors, CROs, and cross-functional teams to drive the success of Phase I-IV clinical trials.

Key Responsibilities

  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for dermatology-focused and multi-therapeutic clinical trials.
  • Conduct medical screenings, dermatological assessments, and physical examinations for study participants.
  • Provide clinical oversight and medical care to study subjects in accordance with protocols, ICH-GCP, and regulatory requirements.
  • Collaborate with study coordinators, nurses, and research staff to ensure compliance and accurate documentation.
  • Document all patient interactions, adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.
  • Establish and maintain strong working relationships with sponsors, CROs, monitors, and IRBs.
  • Participate in site initiation visits (SIVs), monitoring visits, and audits.
  • Contribute to protocol feasibility reviews, study design input, and recruitment strategies.
  • Attend investigator meetings and provide medical expertise on dermatology-related endpoints and safety monitoring.
  • Stay current on clinical research regulations and advances in dermatology and investigational therapies.

Qualifications

  • M.D. or D.O. with an active, unrestricted NC medical license.
  • Board certification in required.
  • Valid DEA license and BLS/ACLS certification.
  • Prior experience in clinical research/clinical trials strongly preferred (training available for motivated candidates).
  • Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).
  • Strong interpersonal and communication skills with the ability to work in a multidisciplinary, fast-paced environment.
  • Commitment to ethical research practices and patient-centered care.

Compensation & Benefits

  • Competitive hourly rate: $100 - $250 based on experience.
  • Flexible part-time schedule.
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About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989

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