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Part Time Clinical Research Monitor Jobs in Raleigh, NC

Support clinical and translational research studies focused on pain management and pain assessment ... monitoring, and maintaining compliance with IACUC protocols and research procedures. * Learn to ...

... clinical research services. We collaborate with top pharmaceutical and biotech companies to ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

... clinical research services. We collaborate with top pharmaceutical and biotech companies to ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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Part Time Clinical Research Monitor information

See Raleigh, NC salary details

$5

$38

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

As of Sep 12, 2026, the average hourly pay for part time clinical research monitor in Raleigh, NC is $37.62, according to ZipRecruiter salary data. Most workers in this role earn between $37.16 and $38.08 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.

What are the most commonly searched types of Clinical Research Monitor jobs in Raleigh, NC?

The most popular types of Clinical Research Monitor jobs in Raleigh, NC are:

What are popular job titles related to Part Time Clinical Research Monitor jobs in Raleigh, NC?

For Part Time Clinical Research Monitor jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Part Time Clinical Research Monitor jobs in Raleigh, NC look for?

The top searched job categories for Part Time Clinical Research Monitor jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Part Time Clinical Research Monitor jobs?

Cities near Raleigh, NC with the most Part Time Clinical Research Monitor job openings:

Infographic showing various Part Time Clinical Research Monitor job openings in Raleigh, NC as of July 2026, with employment types broken down into 100% Part Time. Highlights an 93% In-person, and 7% Remote job distribution, with an average salary of $78,252 per year, or $37.6 per hour.

Clinical Research Dietitian (PT) - Raleigh

Durham, NC

Actalent
Business Management Consulting • 5 - 10K employees

$25 - $50/hr

Part-time, Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Job description

Job Title: Clinical Research Dietitian (Part-Time Hybrid) - Raleigh, NC

Job Description

This part-time Clinical Research Dietitian role offers the opportunity to support participants in a lifestyle-focused clinical research study based in Raleigh. You will guide randomized patients through structured lifestyle management protocols, develop individualized nutrition and exercise goals, and educate them on accurately tracking physical activity and food intake using study-provided materials. Working within clearly defined inclusion and exclusion criteria, you will help determine participant eligibility and contribute to the integrity and success of the research.

Responsibilities

  • Work with randomized study participants as they receive lifestyle management standard operating procedures at 12-week intervals during the study.
  • Develop individualized diet and exercise goals that align with the lifestyle protocol and clinical research requirements.
  • Teach participants how to accurately capture and record physical activity and food intake using study-provided materials and tools.
  • Ensure participant adherence to lifestyle protocols through ongoing guidance, education, and reinforcement of study requirements.
  • Assess and document participant progress at scheduled intervals, providing feedback and adjustments to goals as needed.
  • Apply study inclusion and exclusion criteria to determine whether patients are eligible to participate in the research.
  • Collaborate with the clinical research team to support protocol compliance and high-quality data collection.
  • Interact with principal investigators (PI) and clinical research associates (CRAs) as needed to discuss participant status, protocol questions, and study updates.
  • Maintain accurate, timely, and compliant documentation in accordance with clinical research standards and study protocols.
  • Uphold Good Clinical Practice principles and ethical standards in all participant interactions and study-related activities.

Essential Skills

  • Active North Carolina license as a registered dietitian.
  • Demonstrated experience in nutrition counseling and health education.
  • Ability to develop and implement individualized diet and exercise plans aligned with clinical protocols.
  • Knowledge of clinical research processes and protocol-driven patient management.
  • Strong communication skills to clearly explain lifestyle changes, tracking methods, and study requirements to participants.
  • Ability to teach and coach participants in recording physical activity and dietary intake accurately.
  • Attention to detail when applying inclusion and exclusion criteria for participant eligibility.
  • Capability to work independently in a part-time capacity while coordinating effectively with a research team.

Additional Skills & Qualifications

  • Registered Dietitian credential with eligibility to practice in North Carolina.
  • Good Clinical Practice (GCP) certification is preferred; training can be provided.
  • Experience working in a clinical research setting or with structured lifestyle intervention programs is beneficial.
  • Familiarity with documentation standards and regulatory expectations in clinical research.
  • Comfort interacting with principal investigators and clinical research associates in a professional research environment.
  • Interest in building long-term experience in clinical research within a large site management organization.

Work Environment

This is an on-site, part-time position based in Raleigh, North Carolina, with an expected workload of approximately 10–15 hours per week. The role is performed at a clinical research facility with a flexible schedule, allowing some adaptability in working hours while still meeting study visit and protocol requirements. You will work in a professional healthcare and research environment, collaborating with a multidisciplinary team and using study-provided materials and tools to support participant education and data collection. The setting is designed to support long-term clinical research activities and offers the opportunity to gain substantial experience working within a large, established research infrastructure.

Job Type & Location

This is a Contract position based out of Durham, NC.

Pay and Benefits

The pay range for this position is $25.00 - $50.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Durham,NC.

Application Deadline

This position is anticipated to close on Sep 8, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

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Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Industry

Business management consulting

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

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