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Neurology Rare Disease Center

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Clinical Research Coordinator (CRC)

Flower Mound, TX · On-site

$50K - $70K/yr

Position Summary We are seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trials from start-up through close-out. This role requires ...

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Clinical Research Coordinator I (CRC-1)

Chicago, IL · On-site

$50K - $65K/yr

Director of Clinical Trials and Clinical Research Coordinator III - Team Lead Position Summary The Clinical Research Coordinator I (CRC I) is responsible for supporting the conduct of clinical trials ...

A.P.R., Inc. (AlphaProTemps)

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Clinical Research Coordinator (CRC)

Kalamazoo, MI · On-site

$44/hr

Clinical Research Coordinator (CRC): * For all new Trials, confirm if DTL must be created and if slide deck training is required * Take primary responsibility for early specimen/x-ray/lab submission ...

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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 II

University of Massachusetts Medical School

Worcester, MA

$48K - $58K/yr

Full-time

Re-posted 25 days ago

Job description

POSITION SUMMARY:

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator II is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for complex research protocols related to treatment, ancillary services, and prevention practices.


ESSENTIAL FUNCTIONS:

  • Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA
  • Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
  • Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data
  • Conduct preliminary quality assurance reviews of study data
  • Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe
  • Present study status reports related to assigned research projects
  • Contribute to data presentations and Institutional Review Board (IRB) processes
  • Track and maintain study related information in the data management system within the required timeframe Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs
  • Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • Responsible for monitoring the inventory of research related supplies
  • Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol.
  • Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
  • Comply with all safety and infection control standards appropriate to this position
  • Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices Perform other duties as required.

REQUIRED QUALIFICATIONS:

  • Bachelor’s degree in a scientific or health related field, or equivalent experience
  • 1-3 years of related experience
  • Ability to travel off site locations

CRC Addendum:

Applications are invited for a Clinical Research Coordinator-II (CRC) position at The Eunice Kennedy Shriver Center at UMass Chan Medical School. The CRC will work on multiple projects within the LEAD Lab, under the direction of Dr. Sarabeth Broder-Fingert and in collaboration with other faculty within the Shriver Center.

This position includes work on projects related to NIH- and industry-sponsored research. CRC will support investigations using qualitative interviews with families and professionals as well as quantitative survey data in the study of early development and early identification of children with developmental disabilities, as well as health systems and service access. Projects involve cross-site collaboration and working closely with research partners at other institutions. There will be opportunities for research dissemination, including manuscript preparation and/or conference presentations.

Preferred qualifications:

· Experience with database development and management

· Experience with statistical data analysis

· Comfortable interfacing with families, caregivers, and professionals in the context of recruitment and data collection

· Demonstrated organizational skills and independent problem solving

· Interest in developmental disabilities and health equity

. Proficiency in Spanish

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