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About the Exam

Clinical research certifications validate the knowledge and expertise of professionals working in clinical trials and regulatory compliance.

The two primary certifications covered in Clinops are:

  • SOCRA Certification (CCRP®) – Focuses on Good Clinical Practice (GCP) guidelines, ethical principles, and regulatory frameworks for clinical research professionals.
  • ACRP-CP® Certification – Evaluates knowledge of International Conference on Harmonization (ICH) guidelines and requires verifiable work experience.
These exams assess a candidate’s ability to apply industry standards, regulations, and ethical considerations in clinical research settings.

How Clinops Works

Clinops simplifies exam preparation by offering a structured approach to learning:

  • Curated Question Bank – Access a vast collection of questions tailored to SOCRA and ACRP exams.
  • Exam Simulation – Practice with timed tests to build confidence and improve performance.
  • Progress Tracking Monitor your strengths and focus on areas that need improvement.
  • Accessible Anywhere– Study at your own pace with a user-friendly digital platform.
These exams assess a candidate’s ability to apply industry standards, regulations, and ethical considerations in clinical research settings.

Clinical Research Certifications

Earning a clinical research certification demonstrates your expertise in conducting and managing clinical trials while ensuring compliance with industry regulations and ethical guidelines. The two primary certifications covered in Clinops are:

SOCRA Certification (CCRP®) – Certified Clinical Research Professional

The Certified Clinical Research Professional (CCRP®) certification, offered by the Society of Clinical Research Associates (SOCRA), is designed for individuals involved in clinical trials who want to validate their knowledge of regulatory compliance, Good Clinical Practice (GCP), and ethical considerations.

Key Features:

  • Recognized internationally as a gold standard for clinical research professionals.
  • Covers U.S. Code of Federal Regulations (CFR), ICH Guidelines, and GCP principles.
  • Requires knowledge of ethical research principles, informed consent, trial design, and regulatory requirements.

Who Should Take This Exam?

  • Clinical Research Coordinators (CRCs)
  • Clinical Research Associates (CRAs)
  • Regulatory Specialists & Compliance Officers
  • Study Monitors & Site Managers
  • Data Managers & Clinical Trial Assistants

Eligibility Requirements:

  • At least 2 years of full-time clinical research experience.
  • A degree in a health or science-related field with 1 year of full-time clinical research experience.
  • Completion of an accredited clinical research program with practical experience.

ACRP-CP® Certification – ACRP Certified Professional

The ACRP Certified Professional (ACRP-CP®) certification, offered by the Association of Clinical Research Professionals (ACRP), is designed for experienced clinical research professionals who want to demonstrate their competency in ICH guidelines and clinical trial management.

Key Features:

  • Focuses exclusively on ICH guidelines (does not cover country-specific regulations like FDA or EMA).
  • Requires significant hands-on experience in clinical research.
  • Covers protocol execution, regulatory compliance, and trial oversight.

Who Should Take This Exam?

  • Clinical Research Associates (CRAs)
  • Clinical Trial Managers & Monitors
  • Regulatory Affairs Specialists
  • Quality Assurance Professionals
  • Medical Writers & Data Analysts

Eligibility Requirements:

  • 3,000 hours (approx. 1.5 years) of verifiable work experience in clinical research.
  • Employment in a paid clinical research position (internships do not count).
  • Work related to human subject research.