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Clinical Research Crc Jobs (NOW HIRING)

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

Tekton Research Inc

Clinical Research Coordinator

Wichita, KS · On-site

$21.50 - $28.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented clinical research organization committed to conducting high-quality clinical trials that advance ...

Tekton Research Inc

Clinical Research Coordinator

Henrico, VA · On-site

$22.50 - $29.75/hr

Clinical Research Coordinator (CRC) About Tekton Research: Tekton Research is a growth-oriented clinical research organization committed to conducting high-quality clinical trials that advance ...

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Clinical Research Crc information

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How much do clinical research crc jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical research crc 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 does a clinical research CRC do in clinical research?

A Clinical Research Coordinator (CRC) manages and oversees clinical trial activities, including recruiting participants, obtaining informed consent, collecting data, and ensuring compliance with study protocols and regulatory requirements. They often work closely with investigators, monitor patient safety, and document trial progress using electronic data capture systems. Strong organizational skills and knowledge of Good Clinical Practice (GCP) are essential for this role.

What is a clinical research CRC?

Clinical Research Coordinators (CRCs) are professionals who manage and oversee the daily operations of clinical trials and research studies. They ensure that the study protocols are followed, maintain accurate records, coordinate with research teams and participants, and help ensure compliance with regulatory requirements. CRCs play a vital role in maintaining the integrity of the data collected and in protecting the rights and safety of study participants. Their work is essential to the successful execution of clinical research.

What are some common challenges clinical research coordinators face during clinical trials, and how can they be managed?

Clinical Research Coordinators (CRCs) often face challenges such as managing strict regulatory requirements, coordinating schedules for study participants, and ensuring accurate data collection. Balancing multiple studies and adapting to protocol amendments can also add complexity. To manage these challenges, CRCs rely on strong organizational skills, effective communication with the study team and participants, and staying updated with regulatory guidelines. Utilizing electronic data capture systems and maintaining detailed documentation are also key strategies for success.

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

AspectClinical Research CrcClinical Research Coordinator
CertificationsOften requires GCP, ICH, or CCRP certificationsMay hold similar certifications but less frequently required
Work EnvironmentTypically in clinical trial sites, hospitals, or research facilitiesUsually in hospitals, clinics, or research centers
ResponsibilitiesOversees study compliance, monitors data, manages regulatory documentsCoordinates patient visits, collects data, assists with study procedures
Industry UsageCommonly used in clinical trial settings across pharmaceutical and biotech companiesWidely used in healthcare and research institutions

While both roles are integral to clinical research, the Clinical Research Crc typically has a broader scope involving study oversight and regulatory compliance, whereas the Clinical Research Coordinator focuses more on patient interaction and data collection. Understanding these differences can help you choose the right career path or job search focus.

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

To thrive as a Clinical Research CRC (Clinical Research Coordinator), you need a solid understanding of clinical trial processes, regulatory guidelines, and patient recruitment, usually supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as the Certified Clinical Research Coordinator (CCRC) are often required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills that set top CRCs apart. These abilities ensure accurate study conduct, regulatory compliance, and the successful coordination of research activities.
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Clinical Research Crc jobs near you
Infographic showing various Clinical Research Crc job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Clinical Research Coordinator

GNP Research

Cooper City, FL

$22.25 - $29.50/hr

Full-time

Re-posted 15 days ago

Job description

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and committed to ensuring protocol compliance and participant safety.

Key Responsibilities:

  • Oversee all aspects of clinical trials from start-up to close-out

  • Coordinate patient visits, informed consent, and data collection

  • Ensure regulatory compliance and accurate documentation

  • Liaise with sponsors, CROs, and internal teams

Qualifications:

  • 2+ years of experience as a CRC in a clinical research setting

  • Strong understanding of GCP, FDA regulations, and IRB processes

  • Excellent organizational and communication skills