2

Part Time Clinical Research Associate Jobs (NOW HIRING)

$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 ...

Clinical Research Nephrologist

Arden, NC · On-site

$100 - $250/hr

Job Title: Part-Time Clinical Research Nephrologist 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 ...

Senior Medical Research Associate (Paramedic) - Lenexa, KS (Onsite) ICON is a global healthcare ... We advance clinical research by providing outsourced services to pharmaceutical, biotechnology ...

Senior Medical Research Associate (Paramedic) - Lenexa, KS (Onsite) ICON is a global healthcare ... We advance clinical research by providing outsourced services to pharmaceutical, biotechnology ...

Position Summary The primary responsibility of the Clinical Research Associate I (CRA I) is support ... Annual salaries for part-time positions will be prorated based on the employee's scheduled weekly ...

Showing results 21-40

Part Time Clinical Research Associate information

See salary details

$12

$41

$69

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

As of Sep 5, 2026, the average hourly pay for part time clinical research associate in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is a part time clinical research associate?

Part-time Clinical Research Associates (CRAs) are professionals who monitor and manage clinical trials on a flexible or reduced-hour schedule, rather than full-time. They are responsible for ensuring that studies comply with regulatory requirements, collecting data, and acting as a liaison between clinical trial sites and sponsors. Part-time CRAs may work remotely or travel to research sites as needed, and their schedules can vary depending on the needs of the research project. This role is ideal for those seeking work-life balance or supplementing other professional activities. Their work is critical in advancing medical research and ensuring patient safety.

What are the key skills and qualifications needed to thrive as a part time clinical research associate?

To thrive as a Part Time Clinical Research Associate, you need a background in life sciences or healthcare, knowledge of clinical research protocols, and often a bachelor’s degree in a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certification such as ACRP or SOCRA is highly valued. Strong attention to detail, organizational skills, and effective communication are essential soft skills for monitoring trials and collaborating with research teams. These skills ensure regulatory compliance, accurate data collection, and efficient trial execution, all critical for successful clinical research outcomes.

What are some common challenges faced by part time clinical research associates, and how can they be managed effectively?

Part-time Clinical Research Associates (CRAs) often face the challenge of balancing multiple study sites and projects within limited working hours. Time management and clear communication with both the research team and site staff are crucial to ensure all monitoring visits, documentation, and regulatory requirements are met on schedule. Additionally, part-time CRAs may need to be proactive in staying updated on study protocols and industry regulations, as they may not be present for all in-person team meetings. Establishing structured routines and leveraging digital tools for remote collaboration can help manage these challenges effectively.

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

AspectPart Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often certifications like CCRP or RACBachelor's degree, often certifications like CCRP or RAC
Work EnvironmentMonitoring clinical trials at sites, remote or onsiteManaging trial operations at research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinics
Search & Comparison IntentUnderstanding monitoring roles in trialsManaging trial activities at sites

Part Time Clinical Research Associates primarily focus on monitoring clinical trial progress, ensuring compliance, and verifying data accuracy, often working remotely or onsite. Clinical Research Coordinators handle the day-to-day operations at research sites, including patient recruitment and data collection. Both roles require similar credentials but differ in responsibilities and work settings.

More about Part Time Clinical Research Associate jobs

What cities are hiring for Part Time Clinical Research Associate jobs?

Cities with the most Part Time Clinical Research Associate job openings:

What are the most commonly searched types of Part Time Clinical Research jobs?

The most popular types of Part Time Clinical Research jobs are:

What states have the most Part Time Clinical Research Associate jobs?

States with the most job openings for Part Time Clinical Research Associate jobs include:

Infographic showing various Part Time Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Part-Time Clinical Research Coordinator

Actalent

Albuquerque, NM

$25 - $33/hr

Part-time, Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago


Job description

Job Title: Clinical Research Coordinator – Albuquerque, NM

Job Description

The Clinical Research Coordinator will support and coordinate clinical trial activities for a designated study, working approximately 24 hours per week. This role focuses on patient recruitment efforts such as performing chart review, pre-screening potential participants, and performing community based outreach.

Responsibilities

  • Coordinate day-to-day clinical trial activities for assigned studies in accordance with study protocols and regulatory guidelines.
  • Recruit and screen potential participants for clinical research studies, following approved inclusion and exclusion criteria through chart review.
  • Conduct community outreach efforts to raise awareness of ongoing studies and support participant enrollment.
  • Collaborate with clinical and research staff to ensure smooth study operations and effective communication across the research team.
  • Monitor participant progress and follow up as needed to support protocol compliance and retention.
  • Maintain strict attention to detail in all aspects of study coordination, including documentation, reporting, and communication.
  • Adhere to all applicable ethical, regulatory, and institutional requirements related to clinical research.

Essential Skills

  • Minimum 1+ year of experience working as a Clinical Research Coordinator (CRC).
  • Hands-on experience with clinical trials and clinical research processes.
  • Proficiency with EMR systems.
  • Demonstrated ability to manage patient recruitment activities for clinical studies.
  • Ability to work effectively in a fast-paced environment while managing multiple tasks.

Additional Skills & Qualifications

  • Experience performing community outreach related to clinical research participation.
  • Familiarity with clinical research best practices and regulatory standards.
  • Strong communication and interpersonal skills to interact with participants and research staff.
  • Organizational skills to manage study timelines, documentation, and follow-up activities.
Job Type & Location

This is a Contract position based out of Albuquerque, NM.

Pay and Benefits

The pay range for this position is $25.00 - $33.00/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 fully onsite position in Albuquerque,NM.

Application Deadline

This position is anticipated to close on Sep 9, 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.


Actalent logo

About Actalent

Sourced by ZipRecruiter

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

Social media