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Part Time Clinical Research Monitor Jobs (NOW HIRING)

Protouch Staffing

Clinical Research Cardiologist

Austin, TX · On-site

$100 - $250/hr

Flexible Part-Time (0-8 hours per week) Start Date: Within 0-6 months About the Role We are seeking ... Document patient interactions, monitor adverse events (AEs/SAEs), and maintain compliance with EHR ...

Protouch Staffing

Clinical Research Nephrologist

Austin, TX · On-site

$100 - $250/hr

Flexible Part-Time (0-8 hours per week) Start Date: Within 0-6 months About the Role We are seeking ... Document patient interactions, monitor adverse events (AEs/SAEs), and maintain compliance with EHR ...

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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 Sep 5, 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 is a part time clinical research monitor?

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.

How do part time clinical research monitors 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 the key skills and qualifications needed to thrive as a part time clinical research monitor?

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.

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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Part Time Clinical Research Monitor jobs near you

Clinical Research Dermatologist

Protouch Staffing

Denver, CO • On-site

$180 - $200/hr

Part-time

Re-posted 25 days ago

Job description

Part-Time Gastroenterologist - Clinical Research Physician

???? Denver, CO | ⏰ Part-Time (0-8 hours/week)
Need to have own private practice

About the Role

We are seeking a Board-Certified Gastroenterologist to join as a Clinical Research Physician supporting Phase I-IV clinical trials in Denver, CO. This role involves overseeing protocol compliance, ensuring patient safety, and collaborating with sponsors, CROs, and research teams to advance dermatology-focused and multi-therapeutic studies.

Key Responsibilities

  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.

  • Conduct medical screenings, physical exams, and assessments of study participants.

  • Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.

  • Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.

  • Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.

  • Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.

  • Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.

  • Contribute to feasibility reviews, study design, and recruitment strategies.

  • Provide medical expertise gastro -related endpoints and safety monitoring.

  • Stay current with clinical research regulations and therapeutic advances.

Qualifications

  • M.D. or D.O. with an active, unrestricted CO medical license.

  • Board Certification in Gastroenterologist (required).

  • Valid DEA license and BLS/ACLS certification.

  • Prior experience in clinical research preferred (training available for motivated candidates).

  • Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).

  • Excellent communication, collaboration, and interpersonal skills.

  • Strong commitment to ethical research and patient-centered care.

Benefits

  • Flexible, part-time schedule (0-8 hours per week).

  • Direct involvement in advancing innovative treatments through research.

For More Details: Contact: (469)-290-0934 or Email: asra.moosvi@protouchstaffing.com

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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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