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Part Time Clinical Research Monitor 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 Monitor information

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

As of Jun 15, 2026, the average hourly pay for part time clinical research monitor in the United States is $38.70, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $39.18 per hour, depending on experience, location, and employer.

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

To thrive as a Part Time Clinical Research Monitor, you need a solid understanding of clinical trial protocols, GCP guidelines, and typically a degree in a health-related field. Familiarity with electronic data capture (EDC) systems, regulatory documentation, and possibly certifications like ACRP or SOCRA is advantageous. Strong attention to detail, effective communication, and organizational skills help you manage site visits and collaborate with research teams. These skills ensure protocol compliance, data integrity, and the ethical conduct of clinical studies.

How do part-time clinical research monitors typically balance workload and ensure data quality across multiple studies?

Part-time clinical research monitors often manage their time across several studies by prioritizing tasks, maintaining clear communication with site staff, and using detailed tracking systems. They may face challenges in staying updated on protocol amendments and ensuring timely site visits due to limited hours. To maintain data quality, they frequently collaborate with full-time monitors, utilize remote monitoring tools, and keep thorough documentation. Regular check-ins with the research team help address any issues promptly and ensure compliance with regulatory standards.

What are part time clinical research monitors?

Part time clinical research monitors are professionals who oversee the conduct of clinical trials on a part-time basis. Their primary role is to ensure that research studies comply with regulatory standards, protocols, and ethical guidelines while monitoring participant safety and data integrity. They may visit research sites, review documentation, verify data accuracy, and communicate with investigators, but work fewer hours than full-time monitors. This role is ideal for individuals seeking flexible schedules or supplementary income in the clinical research field.

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

AspectPart Time Clinical Research MonitorPart Time Clinical Trial Coordinator
CredentialsTypically requires life sciences degree, certification (e.g., CCRP), and monitoring experienceUsually requires a degree in health sciences or related field, with project management skills
Work EnvironmentMonitors clinical sites remotely or on-site, ensuring compliance with protocolsCoordinates trial activities, manages documentation, and communicates with sites and sponsors
Employer & Industry UsageCommonly employed by CROs, pharmaceutical companies, and research institutionsEmployed by research sites, hospitals, or sponsors to oversee trial logistics

While both roles support clinical trials, the Part Time Clinical Research Monitor focuses on compliance and monitoring site activities, whereas the Part Time Clinical Trial Coordinator manages trial logistics and documentation. Understanding these differences helps in choosing the right career path or job search focus.

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What cities are hiring for Part Time Clinical Research Monitor jobs? Cities with the most Part Time Clinical Research Monitor job openings:
What are the most commonly searched types of Clinical Research Monitor jobs? The most popular types of Clinical Research Monitor jobs are:
What states have the most Part Time Clinical Research Monitor jobs? States with the most job openings for Part Time Clinical Research Monitor jobs include:
What job categories do people searching Part Time Clinical Research Monitor jobs look for? The top searched job categories for Part Time Clinical Research Monitor jobs are:
Part Time Clinical Research Monitor jobs near you
Part-Time Clinical Research gastroenterologist

Part-Time Clinical Research gastroenterologist

ProTouch Staffing

Asheville, NC

$100 - $250/hr

Part-time

Posted 13 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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