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Ccrp Certification Jobs (NOW HIRING)

UAB

MANAGER-CLINICAL RESEARCH COORDINATION

Tampa, FL · On-site

$77K - $126K/yr

Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) certification strongly preferred. Preferences * Strong leadership and project management skills.

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

CCRC/CCRP certification a plus. Why Join Denali Health: * Work with a mission-driven team advancing clinical research accessibility. * Competitive salary and comprehensive benefits package.

Taphealthcare

Research Nurse Specialist

New York, NY

$109K - $125K/yr

Clinical Research Coordinator (CRC) or Certified Clinical Research Professional (CCRP) certification. * Experience educating patients and coordinating multidisciplinary research activities. Ideal ...

Nationwide Children's Hospital

CCRP certification preferred. Skills: Knowledge of medical terminology and diseases, preferred. Excellent computer skills. Ability to multi-task with strong organizational and prioritization skills.

University of Utah

PS Research Nurse

Campus, IL · On-site

Depending on area of assignment, CCRP, ACRP-CRC, SOCRA-CCRP certification may be required. Current RQI Healthcare Provider eCredential through the University of Utah Health RQI system. The ...

University of Utah

PS Research Nurse

Campus, IL

Depending on area of assignment, CCRP, ACRP-CRC, SOCRA-CCRP certification may be required. Current RQI Healthcare Provider eCredential through the University of Utah Health RQI system. The ...

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How much do ccrp certification jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for ccrp certification in the United States is $26.56, according to ZipRecruiter salary data. Most workers in this role earn between $20.91 and $30.53 per hour, depending on experience, location, and employer.

What is CCRP certification?

CCRP certification stands for Certified Clinical Research Professional. It is a credential awarded by the Society of Clinical Research Associates (SOCRA) to individuals who demonstrate knowledge, experience, and expertise in clinical research. Earning this certification shows that a professional meets industry standards and is committed to maintaining ethical and high-quality clinical research practices. The certification process involves meeting eligibility requirements and passing a comprehensive exam.

What skills and qualifications are needed for CCRP certification?

To thrive as a Clinical Research Professional with CCRP certification, you need a solid understanding of clinical trial protocols, regulatory compliance, and Good Clinical Practice (GCP) guidelines, often supported by a degree in life sciences or healthcare. Familiarity with data management systems, electronic data capture (EDC) tools, and knowledge of regulatory documentation is typically required. Strong attention to detail, organizational skills, and effective communication are critical for coordinating studies and ensuring ethical conduct. These competencies ensure clinical trials are conducted safely, ethically, and in accordance with industry standards, protecting patient welfare and data integrity.

What challenges do professionals face when preparing for CCRP certification, and how can they overcome them?

Professionals preparing for the Certified Clinical Research Professional (CCRP) certification often find balancing study time with full-time job responsibilities challenging, as well as keeping up with the breadth of regulations and ethical guidelines in clinical research. To overcome these challenges, it's helpful to create a structured study schedule, utilize official SOCRA study materials, and join study groups or online forums for peer support. Regularly reviewing real-world case studies can also enhance understanding and retention of complex topics. Many candidates also benefit from attending workshops or webinars offered by professional organizations to clarify difficult concepts.

What is the difference between Ccrp Certification vs Medical Laboratory Technician?

AspectCcrp CertificationMedical Laboratory Technician
Required CredentialsCertification through the American Board for Clinical Pathology (ABCP)Associate degree in medical laboratory technology and certification (e.g., ASCP)
Work EnvironmentClinical laboratories, hospitals, diagnostic labsMedical labs, hospitals, clinics
Industry UsageWidely recognized in clinical pathology and laboratory testingCommon in medical testing and diagnostics

The Ccrp Certification and Medical Laboratory Technician roles both involve laboratory testing, but Ccrp is a certification for professionals overseeing clinical pathology, while Medical Laboratory Technicians perform laboratory tests under supervision. Both are essential in diagnostic labs, with overlapping work environments and industry recognition.

What do you need for Ccrp Certification?

To obtain a CCRP (Certified Clinical Research Professional) certification, candidates typically need a bachelor's degree or higher, relevant clinical research experience, and must pass a certification exam administered by the Society of Clinical Research Associates (SOCRA). Continuing education credits are also required to maintain certification. Specific requirements may vary depending on the certifying organization and the candidate's background.

What is the salary of a clinical research coordinator?

The salary of a clinical research coordinator typically ranges from $50,000 to $70,000 annually, depending on experience, location, and the complexity of the studies they manage. Certification such as CCRP can enhance earning potential, and coordinators often work in clinical or research settings with standard business hours.
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Ccrp Certification jobs near you
Infographic showing various Ccrp Certification job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $55,255 per year, or $26.6 per hour.

Clinical Research Coordinator CRC II

NATIONAL CLINICAL TRIALS INC

Los Angeles, CA • On-site

$26 - $35/hr

Full-time

Retirement, PTO

Re-posted 7 hours ago

Job description

Benefits:
  • 401(k)
  • Paid time off

About the Role:
National Clinical Trials Inc. is looking for a motivated and detail-oriented Clinical Research Coordinator II (CRC II) to join our dynamic team in Los Angeles, CA. In this role, you'll play a critical part in advancing medical research by coordinating and managing clinical trials that make a real difference in patients' lives. If you're passionate about science, patient care, and research excellence, we want to hear from you!
Responsibilities:
  • Coordinate and manage day-to-day operations of clinical trials in compliance with FDA regulations, GCP, and ICH guidelines
  • Screen, enroll, and follow up with study participants while ensuring protocol adherence
  • Collect, record, and maintain accurate study data in EDC systems and source documents
  • Serve as a primary point of contact for sponsors, CROs, and IRB communications
  • Prepare and submit regulatory documents, including IRB submissions, amendments, and continuing reviews
  • Monitor patient safety and report adverse events (AEs) and serious adverse events (SAEs) per protocol requirements
  • Collaborate with principal investigators, sub-investigators, and multidisciplinary clinical teams
  • Support site initiation visits, monitoring visits, and audits conducted by sponsors or regulatory agencies
Requirements:
  • Bachelor's degree in life sciences, healthcare, or a related field required
  • Minimum 2+ years of experience as a Clinical Research Coordinator (CRC)
  • Solid knowledge of GCP, ICH guidelines, FDA regulations, and HIPAA compliance
  • Experience with EDC systems (e.g., REDCap, Medidata Rave) and CTMS platforms
  • ACRP (CCRC) or SOCRA (CCRP) certification preferred
  • Strong organizational skills with exceptional attention to detail and accuracy
  • Excellent interpersonal and communication skills for working with patients and research teams
  • Ability to manage multiple protocols simultaneously in a fast-paced research environment
About Us:
National Clinical Trials Inc. is a leading clinical research organization based in Los Angeles, CA, dedicated to advancing healthcare through innovative and rigorous clinical studies. Our patients trust us for our commitment to safety, integrity, and excellence in every trial we conduct. Our team members thrive in a collaborative, mission-driven environment where their work directly contributes to groundbreaking medical discoveries.