Nationally Certified Clinical Research Professional (NCCRP)
Credential & Job Description Overview
The Nationally Certified Clinical Research Professional™ (NCCRP)™ credential, awarded by the National Clinical Research Certification Association™ (NCRCA™), is a prestigious national certification that recognizes professionals who have demonstrated excellence, competency, and integrity in the conduct of clinical trials and research studies. This credential sets a national benchmark for individuals working in the field of clinical research, ensuring they are well-versed in regulatory compliance, ethical standards, clinical operations, and data integrity.
Credential Description:
The NCCRP™ certification confirms that the professional has completed rigorous training and competency evaluation across the core areas of clinical research, including:
- Good Clinical Practice (GCP)
- Informed consent and participant rights
- Protocol adherence and regulatory documentation
- Clinical trial coordination and data management
- Ethics and compliance with FDA and ICH guidelines
This credential is ideal for individuals in roles such as clinical research coordinators (CRCs), clinical research associates (CRAs), project managers, and others responsible for the oversight, coordination, and implementation of clinical studies.
Certified NCCRP professionals are equipped to operate within diverse research settings and demonstrate leadership in conducting safe, ethical, and compliant research involving human subjects.
NCRCA Credential Overview – NCCRP Nationally Certified Clinical Research Professional
NCCRP – Nationally Certified Clinical Research Professional
Credential Description
This credential certifies experienced professionals responsible for coordinating, managing, and executing key elements of clinical trials across multiple phases.
Job Analysis
– Study Coordination: Manage daily study activities and participant visits
– Regulatory Compliance: Ensure trials follow GCP, IRB, and sponsor requirements – Participant Interaction: Educate, consent, and monitor research subjects
– Documentation: Maintain case report forms and protocol logs
Eligibility Requirements
– Employed by NCRCA-accredited partner employer
– OR complete 1-Day National Certification Bridge Program – OR attend an NCRCA-hosted Certification Conference
Exam Format
100 multiple-choice questions
Exam Content Breakdown
– Study Management & Coordination – 35% – Participant Oversight & Consent – 25%
– Regulatory & Protocol Compliance – 20% – Clinical Data & Documentation – 10%
– Ethical Conduct & Communication – 10%
Initial Certification Fee
$398
Annual Maintenance Fee
$398
Renewal Requirements
– 500 hours verified employment
NCRCA Credential Overview – NCCRP Nationally Certified Clinical Research Professional
– 10 CE hours related to the role
– $398 renewal fee submitted before expiration