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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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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.

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:
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

CLINICAL RESEARCH COORDINATOR I (PART-TIME) (DEMOPOLIS, AL)

UAB NOVA RENT

Birmingham, AL • On-site

$21.10 - $34.30/hr

Part-time

Posted 17 days ago

Job description

The University of Alabama at Birmingham (UAB), General Internal Med & Population Science, is seeking a Clinical Research Coordinator I (Part-Time).
The Part-time Clinical Research Coordinator I will assist with small and large scale clinical studies and trials in the community of Demopolis, AL. Principle responsibilities include education, recruitment, patient navigation and retention efforts, data quality control and regulatory compliance.
General Responsibilities
  • To collect and record preliminary data for clinical research programs.
  • To recruit and perform follow-up with research participants as protocols outline.
  • To schedule visits according to research protocols.
  • To assist in coordination of lab and fieldwork.
  • To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.

Key Duties & Responsibilities
  1. Serves as coordinator for studies and initiatives and provides support to other team members within the confines of the protocol as directed.
  2. Supports screening and participant eligibility determination, consent, enrollment, survey, and provides health education and navigation services.
  3. Conducts activities in accordance with the protocol, regulations and Good Clinical Practice (GCP).
  4. Assists with the study life cycle from start-up to closure, i.e., collecting and recording data, recruiting and performing follow-up with participants, scheduling visits, and assisting in the coordination of lab and fieldwork.
  5. Performs other duties as assigned.

Hourly Range : $21.10 - $34.30
Qualifications
High School diploma or GED required.
Preferences
  • Ability to operate various office machines, including printers, computers, and various software packages.
  • Interpersonal skills.
  • Knowledge of Microsoft Office products.
  • Written and verbal communication skills.
  • Data entry skills.

UAB is an Equal Employment/Equal Educational Opportunity Institution dedicated to providing equal opportunities and equal access to all individuals regardless of race, color, religion, ethnic or national origin, sex (including pregnancy), genetic information, age, disability, and veteran's status. As required by Title IX, UAB prohibits sex discrimination in any education program or activity that it operates. Individuals may report concerns or questions to UAB's Assistant Vice President and Senior Title IX Coordinator. The Title IX notice of nondiscrimination is located at uab.edu/titleix.

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