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Clinical Research Volunteer Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Sioux Falls, SD · On-site

$35 - $42/hr

Clinical Research Coordinator - Sioux Falls, SD Work Setup: On-site Schedule: Part-time (24 hours ... Recruit, screen, and orient volunteers while prioritizing their safety and well-being * Collect and ...

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Clinical Research Volunteer information

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How much do clinical research volunteer jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical research volunteer in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is a clinical research volunteer?

Clinical research volunteers are individuals who participate in medical studies or clinical trials to help researchers gather data about new treatments, medications, or procedures. Their involvement is essential for advancing medical knowledge and ensuring the safety and effectiveness of new interventions. Volunteers may be healthy individuals or patients with specific conditions, and participation is typically voluntary and guided by ethical standards to protect their rights and well-being.

What types of tasks and responsibilities can I expect as a clinical research volunteer?

As a Clinical Research Volunteer, you may support research staff by assisting with data collection, preparing study materials, helping with participant recruitment, and maintaining accurate records. Your responsibilities might also include scheduling appointments, handling basic administrative tasks, and ensuring compliance with study protocols. This role provides valuable exposure to clinical research methods and often involves close collaboration with research coordinators, investigators, and healthcare professionals, offering insights into the day-to-day operations of clinical trials.

What are the key skills and qualifications needed to thrive as a clinical research volunteer, and why are they important?

To thrive as a Clinical Research Volunteer, you need a basic understanding of scientific research principles, strong organizational skills, and often a background in life sciences or related fields. Familiarity with data entry software, electronic data capture (EDC) systems, and standard research protocols is commonly expected. Attention to detail, teamwork, and effective communication are standout soft skills in this role. These abilities ensure accurate data collection, adherence to ethical standards, and successful collaboration within research teams.

What is the difference between Clinical Research Volunteer vs Clinical Research Coordinator?

AspectClinical Research VolunteerClinical Research Coordinator
Required CredentialsTypically no formal credentials; some may have basic health or research trainingUsually requires a degree in health, life sciences, or related field; certification may be preferred
Work EnvironmentResearch sites, hospitals, clinics; volunteer basisResearch sites, hospitals; paid position with more responsibilities
Employer & Industry UsageNon-profit organizations, academic institutions, research companiesPharmaceutical companies, academic research centers, hospitals
Common Search & Comparison IntentUnderstanding volunteer roles in clinical trialsLearning about paid positions managing clinical studies

The main difference between a Clinical Research Volunteer and a Clinical Research Coordinator is that volunteers typically assist with research without formal credentials and on a volunteer basis, while coordinators are paid professionals with relevant education and responsibilities managing clinical trials.

What cities are hiring for Clinical Research Volunteer jobs?

Cities with the most Clinical Research Volunteer job openings:

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

The most popular types of Clinical Research jobs are:

What states have the most Clinical Research Volunteer jobs?

States with the most job openings for Clinical Research Volunteer jobs include:

Clinical Research Volunteer jobs near you
Infographic showing various Clinical Research Volunteer job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Clinical Research Coordinator

Odyssey Systems Consulting Group, Ltd.

Fort Liberty, NC

$20.50 - $27.25/hr

Full-time

Re-posted 21 days ago

Job description

Odyssey is looking for a Clinical Research Coordinator to coordinate and assure the integrity of all activities associated with conducting Traumatic Brain Injury Center of Excellence (TBICoE) clinical investigations in TBI, brain health, and related outcomes. The candidate will ensure compliance with local, state, and/or federal regulatory requirements. This job is onsite at Ft Bragg, NC.

***Contingent upon contract award***


Duties include, but are not limited to:

  • Coordinates and assures integrity of all activities associated with conducting TBICoE TBI clinical investigations as it relates to compliance with local, state, and/or federal regulatory requirements.
  • Assists Principal / Associate Investigators in the preparation and submission of clinical protocols, consent forms and other documents to the scientific review committee, IRB and other regulatory organizations.
  • Prepares requests for actions/proposals to include assisting with and providing coordination for grant proposal applications and their associated documentations and requirements as Facilitates the flow and approval processes for relevant projects as needed or requested.
  • Maintains regulatory files related to TBICoE clinical investigations.
  • Communicates with research participants, staff, regulatory affairs and data management groups, laboratory and clinical investigators, management and outside collaborators.
  • Recruits, interviews, and screens TBICoE clinical research study volunteers, administers and obtains informed consent
  • Assists in the collection and analysis of data to evaluate volunteer eligibility for enrollment.
  • Assists with TBI Program/Quality Improvement initiatives or implementation science studies.
  • Assists in the collection, analysis and interpretation of laboratory and clinical data obtained during a medical evaluation, report significant values, findings and events that require prompt attention to clinical investigators.
  • Assists with the documentation and reporting of adverse events, completes and reviews subject eligibility criteria, protocol compliance, omissions, and errors and submits these forms as
  • Prepares and maintains written and electronic volunteer databases/logs.
  • Performs data extraction and chart reviews of patients’ and/or research participant’s medical records or other relevant record/systems, as applicable.
  • Ensures that research records are stored and secured properly and that inventory and records are updated and properly maintained.
  • Conducts data verification as indicated, documents, assists the investigator and protocol coordinator with questions, may transcribe and resolve queries of data on study forms (hardcopy and/or electronic).
  • Prepares documents, under direction of project leads. Trains incoming staff on study procedures and SOPs.
  • Assists with statistical analyses and descriptive data capture under direction of project leads. Works with the site senior clinical research director and other senior research leads for the collection, documentation and analysis of metrics to ensure a successful research program.

***Contingent upon contract award***


Minimum Required Qualifications

Citizenship: Must be a US citizen.

Clearance:  Ability to Obtain Secret.

Education:  Bachelor's Degree or higher in biology, psychology or related health/social science required. Master’s degree preferred. Must have Human Subjects training completed.

Years of Experience:  3-5 years clinical investigations experience required. Prior experience within the DoD/VA systems of care preferred.

Certifications:   Certification as a Clinical Research Coordinator (CCRC), Clinical Research Professional (CCRP) and/or Clinical Research Associate (CCRA) preferred (must maintain Continuing Education credit sufficient to maintain certification when applicable).

Other requirements:

  • Excellent communication skills, basic clinical acumen, knowledge of universal precautions, organizational skills and proficiency in research conduct are required.
  • Knowledge of standard qualitative and quantitative data collection techniques; ability to follow general instructions; works effectively in a team and independently; demonstrates strong communication, writing and analytical skills. Familiarity with social science research methodology is required. Ability to follow detailed instructions.
  • Must be able to work comfortably with computer software, including Microsoft Office and familiarity with basic statistical analyses.
  • Adhere to legal, professional and ethical codes with respect to confidentiality and privacy.
  • Physical Capabilities: Must be able to sit and stand for long periods of time. Must be able to carry light items – up to 25 lbs.
  • Work Environment: Office clinical and hospital environment. May encounter patients who are confused, agitated or abusive.
  • Must be available to travel locally, regionally and nationally. May include hours in the late afternoons, evenings, and/or weekends, depending on study assessments and participant scheduling requirements.

Additional Information

Location: Naval Medical Center San Diego, 34800 Bob Wilson Drive, San Diego, CA.

Travel: NA

Remote, Onsite, or Hybrid: Onsite

#LI-JC1

***Contingent upon contract award***


Odyssey is a world-class technical, engineering, and integration company serving the warfighting ecosystem with airborne integration, ISR, C2, and warfighter readiness capabilities. Odyssey meets the military’s operational needs by integrating layered defense systems from equipment, technology, and services to data, information, and business operations. We streamline defense acquisition and sustainment, engineering the technical battlefield with domain-specific proficiency to ensure lethality. Odyssey is dedicated to excellent contract execution, peak organizational performance, and fostering a workplace built on employee care.

Odyssey is proud to live out our core values of commitment, ambition, and respect in our work and communities through OdysseyCares, a philanthropic group focused on giving back through direct donations, an employer match program, and volunteering events.

Please note: Final compensation for this position will be determined by various factors such as the Federal Government contract labor categories and contract wage rates, relevant work experience, specific skills and competencies, geographic location, education, and certifications.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities


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