2

Part Time Clinical Research Associate Jobs in Tennessee

Clinical Trial Nurse

Nashville, TN · On-site

$50 - $60/hr

Exposure to clinical research and trial operations * Competitive perdiem compensation Additional ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Clinical Staff Pharmacist

Nashville, TN · On-site

$54.25 - $60.50/hr

To provide access to high-quality cancer care and the expertise of clinical research for all ... Actively participate in Pharmacy & Therapeutics (P&T) Committee decisions and support the ...

MedTech

Nashville, TN · On-site

$39 - $42/hr

IQVIA is a leading global provider of clinical research services, commercial insights and health ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

next page

Showing results 1-20

Part Time Clinical Research Associate information

See Tennessee salary details

$10

$37

$63

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

As of Aug 29, 2026, the average hourly pay for part time clinical research associate in Tennessee is $37.33, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $47.79 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.

What are popular job titles related to Part Time Clinical Research Associate jobs in Tennessee?

For Part Time Clinical Research Associate jobs in Tennessee, the most frequently searched job titles are:

What job categories do people searching Part Time Clinical Research Associate jobs in Tennessee look for?

The top searched job categories for Part Time Clinical Research Associate jobs in Tennessee are:

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

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

Infographic showing various Part Time Clinical Research Associate job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $77,639 per year, or $37.3 per hour.

Part-Time Clinical Research Coordinator

Chattanooga, TN

Actalent
Business Management Consulting • 5 - 10K employees

$25 - $35/hr

Part-time, Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 2 days ago

New


Job description

Job Title: Hybrid Part-Time Clinical Research Coordinator

Job Description

This Clinical Research Coordinator role supports a clinical trial at a research site in the Chattanooga, TN area. You will identify and recruit eligible participants, educate them about the study, and help ensure they remain engaged and compliant throughout the trial. The position requires strong clinical research experience, excellent organizational skills, and the ability to communicate confidently with both participants and research staff. This is a 24-hour-per-week role. It is a flexible position with a majority of the hours remote or hybrid.

Responsibilities

  • Identify, pre-screen, and recruit eligible participants for the clinical trial through community outreach and other recruitment strategies.
  • Perform patient recruitment activities, including phone screening, in-person discussions, and follow-up communication to support enrollment goals.
  • Conduct community outreach efforts to spread awareness of the study, including visiting local community locations and attending community events.
  • Partner with local clinics, medical practices, and medical professionals to generate patient referrals for the clinical trial.
  • Educate healthcare providers about the clinical trial, including study objectives, eligibility criteria, and participant qualifications.
  • Explain study procedures, expectations, and requirements to potential participants in a clear and empathetic manner.
  • Support participants throughout the trial to promote engagement, adherence, and protocol compliance.
  • Collaborate closely with research staff and investigators to ensure accurate and timely execution of study-related activities.
  • Use electronic medical records (EMR) systems to review patient information, support pre-screening, and document recruitment activities.
  • Follow Good Clinical Practice (GCP) guidelines and privacy regulations to protect participant safety and confidentiality.
  • Maintain organized documentation of recruitment efforts, participant interactions, and study-related records.
  • Contribute to a fast-paced research environment by managing multiple tasks and priorities with strong attention to detail.

Essential Skills

  • Proven experience as a Clinical Research Coordinator or Clinical Research Experience.
  • At least 1+ year of experience in patient recruitment for clinical research or clinical trials.
  • Clinical research experience, including familiarity with clinical trial processes and protocols.
  • Training in HIPAA regulations and patient privacy requirements.
  • Training in Good Clinical Practice (GCP).
  • Strong organizational skills with the ability to manage multiple tasks and deadlines.
  • Confident verbal and written communication skills for interacting with participants, providers, and research staff.
  • Ability to work effectively in a fast-paced environment while maintaining accuracy and attention to detail.
Job Type & Location

This is a Contract position based out of Chattanooga, TN.

Pay and Benefits

The pay range for this position is $25.00 - $35.00/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 Chattanooga,TN.

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