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Volunteer Weekend Clinical Research Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Sioux Falls, SD

$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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Volunteer Weekend Clinical Research information

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How much do volunteer weekend clinical research jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for volunteer weekend clinical research 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 the difference between Volunteer Weekend Clinical Research vs Clinical Research Coordinator?

AspectVolunteer Weekend Clinical ResearchClinical Research Coordinator
CredentialsTypically no formal credentials requiredOften requires a degree in health sciences or related field
Work EnvironmentVolunteer settings, part-time, weekendsFull-time, clinical or hospital settings
Employer & IndustryResearch institutions, nonprofits, universitiesHospitals, pharmaceutical companies, research centers
Search & Comparison IntentUnderstanding volunteer roles in clinical researchExploring career paths in clinical research management

Volunteer Weekend Clinical Research roles typically involve assisting in research activities without formal credentials, often during weekends. Clinical Research Coordinators are paid professionals with relevant education, managing clinical trials full-time. The roles differ mainly in responsibilities, credentials, and work environment, but both are integral to the clinical research industry.

What cities are hiring for Volunteer Weekend Clinical Research jobs?

Cities with the most Volunteer Weekend Clinical Research job openings:

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

The most popular types of Weekend Clinical Research jobs are:

What states have the most Volunteer Weekend Clinical Research jobs?

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

Volunteer Weekend Clinical Research jobs near you
Infographic showing various Volunteer Weekend Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Senior Clinical Research Coordinator

Headlands Research

Riverside, CA • On-site

$85K - $90K/yr

Full-time

Re-posted 3 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Riverside, CA
Artemis Institute for Clinical Research (a Headlands Research site)
Full-time | Onsite (no opportunities for hybrid or remote)
For experienced CRCs looking for stability, collaboration, and meaningful work
If you're an experienced Clinical Research Coordinator who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work-life balance, Artemis Institute for Clinical Research may be the right next step in your career.
Our Riverside site is known for its depth of experience, thoughtful study execution, and team-based approach to clinical research-particularly in vaccines, CNS, general medicine, and psychiatry.
About Artemis Institute for Clinical Research
Artemis Institute for Clinical Research in Riverside is a patient-centered clinical research site and part of the Headlands Research family. Founded with a core mission to prioritize patients, advance medicine, and improve the world, Artemis combines rigorous, process-driven trial management with a compassionate approach to care. The site conducts high-quality clinical trials across multiple therapeutic areas-including psychiatric, metabolic, vaccine, and healthy volunteer studies-and has helped thousands of participants contribute to meaningful medical advancements. Artemis is known for its collaborative team culture, strong operational standards, and commitment to excellence in delivering reliable, protocol-compliant research on behalf of pharmaceutical and biotech sponsors.
Why Experienced CRCs Choose Artemis
  • Multi-disciplinary collaboration with seasoned investigators and clinical staff
  • Strong operational support and clear SOPs
  • Exposure to complex, meaningful studies-not just high-volume turnover
  • Backing of a growing research network with resources and stability

This role is ideal for CRCs who enjoy owning their studies, working with competent teams, and being trusted to execute with precision.
Responsibilities:
  • Provide the highest level of care for study patients
  • Deliver excellent customer service to pharmaceutical clients
  • Coordinate all aspects of assigned clinical trials from site initiation through close-out
  • Conduct subject visits and ensure accurate, timely documentation in compliance with protocol and standards
  • Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs
  • Manage subject recruitment, informed consent, and retention activities
  • Ensure timely EDC data entry and resolution of queries
  • Report and follow up on AEs, SAEs, and protocol deviations
  • Collaborate with investigators, sponsors/CROs, labs, and internal teams
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure training compliance for amendments and systems
  • Perform study procedures such as phlebotomy, ECGs, and sample processing (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of protocols, lab manuals, equipment calibration, and inventory

Requirements:
  • At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required
  • High school diploma or GED required
  • Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations
  • Experience with EDC, IVRS, and clinical research platforms
  • Proficiency in medical terminology and clinical documentation
  • Strong organizational skills with the ability to manage multiple studies
  • Clear, professional verbal and written communication skills
  • Comfortable working onsite in a collaborative, clinical environment

Who Thrives in This Role
  • CRCs who want structure, support, and accountability
  • Those interested in taking the next step in managing people
  • Professionals who value teamwork over silos
  • Coordinators who care about data quality, patient experience, and compliance
  • Those ready to grow within a stable, well-established research site

Apply today if you're looking for a CRC role where your experience is respected, your schedule is predictable, and your work directly contributes to advancing meaningful medical research.
California Pay Range
$85,000-$90,000 USD
Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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