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Part Time Clinical Research Organization 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 ... organizational skills. Prior experience in humans subjects research is required, and prior ...

Access Community Clinical Trials

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Clinical Research Nurse

Abilene, TX · On-site

Abilene, Texas Employment Type: Part-Time Access Community Clinical Trials (ACCT) is a growing clinical research organization dedicated to expanding access to high-quality clinical trials within ...

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As of Jun 16, 2026, the average hourly pay for part time clinical research organization in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.
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Part-Time Clinical Research gastroenterologist

Part-Time Clinical Research gastroenterologist

ProTouch Staffing

Asheville, NC

$100 - $250/hr

Part-time

Posted 14 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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