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Clinical Research Crc Jobs (NOW HIRING)

One of a Kind Clinical Research Center LLC

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Clinical Research Coordinator (CRC)

Kingwood, TX · On-site

$23 - $28/hr

Clinical Research Coordinator (CRC) Kingwood, Texas | On-site We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to join our team in Kingwood, TX. This position is ...

LINQ Research, LLC

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Clinical Research Coordinator (CRC)

Pearland, TX · On-site

$58K - $65K/yr

Clinical Research Coordinator (CRC) LINQ Research, LLC Location: Pearland, TX -0 Onsite Job Type: Full-Time Schedule: Monday-Friday, 8:00 AM-5:00 PM Department: Clinical Research Reports To: Site ...

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 ...

Insight

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 ...

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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 (CRC)

One of a Kind Clinical Research Center LLC

Kingwood, TX • On-site

$23 - $28/hr

Full-time

Medical, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Clinical Research Coordinator (CRC)
Kingwood, Texas | On-site

We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to join our team in Kingwood, TX. This position is embedded within a clinical practice and offers the opportunity to work closely with patients, physicians, and research teams to advance clinical trials.

This role is ideal for someone who is self-driven, thrives in a collaborative environment, and is excited about contributing to cutting-edge clinical research.

Key Responsibilities:

  • Coordinate and manage clinical trial activities from start-up through close-out
  • Recruit, screen, and enroll study participants
  • Conduct patient visits in accordance with study protocols
  • Perform clinical assessments and collect study data
  • Assist with and support surgical procedures as required by protocol
  • Maintain accurate and timely source documentation and regulatory files
  • Ensure compliance with protocol, sponsor requirements, and regulatory guidelines
  • Manage study-related administrative tasks, including data entry and query resolution
  • Communicate effectively with investigators, sponsors, and study participants

Qualifications:

  • Previous experience as a Clinical Research Coordinator preferred (or relevant healthcare/research experience)
  • Strong organizational skills and attention to detail
  • Ability to work independently while contributing to a team environment
  • Excellent communication and patient-facing skills
  • Comfortable in a fast-paced clinical setting
  • Experience with EMR systems and clinical trial documentation a plus
  • Phlebotomy, EKG, or other clinical skills preferred (if applicable)

What We’re Looking For:

  • Self-motivated and proactive mindset
  • Strong sense of ownership and accountability
  • Team player with a positive attitude
  • Passion for clinical research and patient care
  • Experience in patient care and clinical trials

Why Join Us:

  • Opportunity to be part of a growing research program within an established clinic
  • Hands-on experience across a variety of studies and procedures
  • Collaborative and supportive team environment
  • Meaningful impact on patient care and medical advancement

Company Description

One of a Kind Clinical Research is a growing clinical trial site dedicated to advancing medicine across multiple therapeutic areas. We partner with sponsors and patients alike to deliver high-quality research with a personal touch. As a newer site, we move with purpose and passion — building a team that's collaborative, community-connected, and committed to making a real impact in the world of clinical research.