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Part Time Clinical Research Monitor Jobs (NOW HIRING)

University of Pennsylvania

$22.36 - $22.75/hr

... part-time Clinical Research Coordinator (CRC). The candidate will help coordinate an industry ... monitoring plan reports; maintaining study charts; and entering study data. The Center for Weight ...

University of Pennsylvania

$22.36 - $22.75/hr

... part-time Clinical Research Coordinator (CRC). The candidate will help coordinate an industry ... monitoring plan reports; maintaining study charts; and entering study data. The Center for Weight ...

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Part Time Clinical Research Monitor information

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$39

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

As of Jul 6, 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.

More about Part Time Clinical Research Monitor jobs
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:
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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
Clinical Research Coordinator I (Temporary/Part-Time)

Clinical Research Coordinator I (Temporary/Part-Time)

INBIOS INTERNATIONAL INC

Seattle, WA • On-site

$26.44 - $31.25/hr

Part-time, Temporary

Medical, Dental, Vision, Life, Retirement

Posted 24 days ago

Job description

Description:

Are you a detail-oriented problem-solver with a passion for purpose-driven work? Join InBios, a mission-focused biotech company developing diagnostic tools that combat infectious diseases worldwide.


About Us

InBios International Inc. has been in business since 1996 designing and manufacturing diagnostic assays for emerging infectious diseases and biothreats. Our work supports global health initiatives and government-funded research, with a strong emphasis on innovation, quality, and compliance. Based in Seattle, we offer a collaborative culture, competitive compensation, and meaningful work that makes a global impact.


Location: Seattle, WA


Type: Part-Time (30 hours per week), Temporary (6-months) | Hybrid
This is a project-based position funded by a federal contract. If selected for the position, you will be hired as a temporary, part-time employee and the term of employment is dependent upon ongoing funding.


Position Wage Range: $26.44 – $31.25/per hour


What You’ll Do

We're looking for a temporary, part-time Clinical Research Coordinator to support clinical studies and international product registration. The successful candidate must have a BS in a scientific discipline, have familiarity with Good Clinical Practice (GCP) and have excellent attention to details as well as good communication skills but written and verbal.


Key ResponsibilitiesClinical Site Monitoring
  • Under the direction of the Project Manager assist in the maintenance of regulatory binders and Institutional Review Board (IRB) submissions.
  • Monitor clinical study to ensure that all participant records entered into the electronic data capture system are accurate and follow the clinical protocol and source documents.
  • Participate in Site Initiation training (SIV), monitor study compliance, and assist with study closeout.
  • Ensure that participants enrolled in the study meet the inclusion/exclusion criteria.
  • Monitor and report protocol deviations and adverse events in a timely manner.
  • Participate in study site close-out.
Product Registrations (International)
  • Identify regulatory requirements for product registrations worldwide.
  • Review analytical and clinical data against country regulatory requirements and identify gaps that need to be filled to obtain product registration.
  • Assist in the preparation of technical files in compliance with IVDR.
What We’re Looking ForRequired
  • Bachelor’s degree in a scientific discipline.
  • Strong attention to detail, excellent written and verbal communication, and proficiency with technology (e.g., MS Office, Electronic Database Systems).
  • Knowledge of ICH GCP guidelines. GCP certification.
  • Entry-level knowledge of IVDR requirements for medical devices.
Preferred
  • 1- to 3-year experience in project management.
  • Certified Clinical Research Associate credential.
Perks & Benefits
  • Medical, dental, vision, life & disability insurance
  • 401(k) + Roth IRA + FSA
  • Prorated paid holidays and sick time as applicable to term of employment and work schedule in accordance with policies stated in the Company’s employee handbook.
  • Supportive, mission-driven culture


Apply Today

Be part of a team that’s advancing science and improving lives.

Requirements: