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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 ...

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Clinical Research Crc information

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How much do clinical research crc jobs pay per hour?

As of Sep 5, 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 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 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.

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 states have the most Clinical Research Crc jobs?

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

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 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

Tandem Clinical Research

Melbourne, FL • On-site

$22.50 - $30/hr

Full-time

Re-posted 7 days ago

Job description

Clinical Research Coordinator (CRC)
The Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards.
The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.
Key Responsibilities
Study Management & Coordination
  • Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
  • Support study start-up activities including feasibility, regulatory submissions, and site activation.
  • Attend investigator meetings, site initiation visits, and other study-related meetings.
  • Manage visit schedules and coordinate study-related activities across clinical teams.

Recruitment, Enrollment & Consent
  • Collaborate with recruitment teams to support participant screening and enrollment.
  • Conduct informed consent discussions with participants, ensuring understanding of study requirements and documentation of consent.
  • Ensure protocol and regulatory requirements are met throughout the enrollment process.

Clinical Oversight & Subject Monitoring
  • Monitor and assess study subjects in accordance with protocol requirements.
  • Identify, document, and report adverse events in collaboration with the Principal Investigator and clinical staff.
  • Escalate safety concerns and protocol issues to the PI, sponsor, and IRB as required.

Documentation, Data & Systems
  • Maintain accurate and complete source documentation, case report forms, regulatory files, and study records.
  • Enter study data into EDC and other required systems and manage study databases.
  • Complete, verify, and resolve case report forms and sponsor or monitor queries in a timely manner.
  • Report protocol deviations to the PI, sponsor, and IRB as required.

Investigational Product & Specimen Management
  • Manage investigational product accountability records and documentation.
  • Collect, process, package, and ship study specimens per protocol requirements.
  • Perform phlebotomy and handle biological specimens in accordance with study protocols and safety guidelines, when trained and authorized.

Quality, Compliance & Team Support
  • Ensure all study activities comply with SOPs, GCP, and regulatory requirements.
  • Support quality assurance activities and audit readiness.
  • Provide assistance and mentorship to fellow coordinators as needed.
  • Maintain strict confidentiality of participant and study information.

Communication & Outreach
  • Serve as the primary point of contact for sponsor and CRO communications.
  • Participate in occasional outreach or community events related to clinical trials.
  • Ensure timely, accurate communication of study updates and issues.

Additional Responsibilities
This job description outlines the primary responsibilities of the Clinical Research Coordinator but is not exhaustive. Additional duties may be assigned as needed to support study requirements, operational needs, and organizational priorities. Responsibilities may evolve based on protocol complexity and business needs.
Requirements
  • Knowledge, Skills, and Abilities
  • Strong leadership and communication skills
  • Exceptional organizational and multitasking abilities
  • High attention to detail and commitment to regulatory compliance
  • Ability to work independently and collaboratively in a multidisciplinary environment
  • Strong time management and operational efficiency skills
  • Proficiency with office equipment and study-specific systems
  • Ability to maintain strict confidentiality
  • Required Experience & Qualifications
  • Education: Bachelor's degree in a related field
  • Experience: Minimum of two (2) years of clinical research or clinical trial management experience
  • Preferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN)
  • Phlebotomy: Prior experience performing blood draws and handling biological specimens required

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