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Clara Fargo
EBMT Clinical Research Quality Assurance Coordinator
I have finalised the demo for the ICH-GCP E6 R3 refresher course. Overall, I liked the content and the interface. I also want to thank Whitehall Train...
Clinical Research Associate (CRA)
4.3
★★★★★
94% Recommended
Updated 2025
21 hours
126 active users
21 points
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Each course includes:
Fully compliant
This course meets the required standard for basic GCP training, allowing learners to work on clinical trials. Learners also receive 6 Continuing Professional Development (CPD) Points awarded by the Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom. These can be used to count towards the distance learning element of any scheme that comes under the umbrella of The Academy of Medical Royal Colleges or any other scheme for which there is mutual recognition.
Certified
All learners who pass the final exam receive a uniquely numbered, personal certificate to demonstrate their subject knowledge. Since the questions are picked randomly from database, re-sitting the exam doesn’t mean taking the same questions again and again.
Affordable
Our cost-effective prices represent excellent value. You can easily pay up to ten-times more for face-to-face training. We can also offer generous group discounts on larger purchases.
Time-saving
Our new administration system makes it incredibly quick and simple to allocate licences to multiple learners. Learners save time too by choosing when and where they complete the training.
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About
The CRA – Essentials Learning Path is a structured foundational program designed to equip learners with the core knowledge and practical understanding required for a Clinical Research Associate (CRA) role. This learning path covers the regulatory, ethical, operational, and documentation aspects of clinical trials, ensuring alignment with global clinical research standards.
The program provides a strong grounding in Good Clinical Practice (GCP), clinical trial fundamentals, data privacy regulations, and Good Documentation Practices (GDocP)—all critical to ensuring subject safety, data integrity, and regulatory compliance. In addition, the learning path introduces the application of Artificial Intelligence (AI) in clinical research, helping learners understand emerging technologies shaping the future of clinical trials.
Designed for both new entrants and professionals transitioning into clinical research, this learning path prepares learners to support site monitoring, trial oversight, regulatory inspections, and compliant trial execution across sponsors, CROs, and investigative sites.
Who Should Enrol?
- Aspiring Clinical Research Associates (CRAs) looking to build a strong foundation in clinical research.
- Life sciences and pharmacy graduates seeking to enter the clinical research industry.
- Clinical Trial Coordinators (CTCs), site staff, and research professionals involved in clinical trial operations.
- Healthcare, quality assurance, and regulatory professionals transitioning into clinical research, as well as junior CRAs seeking a structured refresher of core concepts.
What you will learn
Understand the fundamentals of clinical research, clinical trial monitoring, and the role of a Clinical Research Associate (CRA) in ensuring study quality and compliance.
Learn the key principles of clinical trial documentation, site management, and regulatory requirements in global clinical research.
Develop knowledge of Good Clinical Practice (GCP), ethical guidelines, and compliance processes that support successful clinical trial conduct.
Gain the foundational skills and regulatory awareness needed to contribute to monitoring, documentation, and compliance activities across clinical studies.
Courses Included
Introduces the roles, responsibilities, and day-to-day activities of a Clinical Research Associate across the clinical trial lifecycle
2 hours
2 points
Reinforces core Good Clinical Practice principles, ethical standards, and regulatory responsibilities essential for compliant clinical trial conduct
3 hours3 points
Covers key concepts of clinical research including trial phases, study design, protocols, stakeholders, and trial execution processes
3 hours3 points
Covers the HIPAA Privacy Rule, Security Rule, and other relevant regulations to ensure compliance with the Health Insurance Portability and Accountability Act (HIPAA)
4 hours4 points
Focuses on accurate, complete, and compliant documentation practices to ensure data integrity and inspection readiness
3 hours3 points
Introduces the use of artificial intelligence in clinical trials, including data management, monitoring efficiencies, and risk-based approaches
6 hours6 pointsOur Certified Customers
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Frequently Asked Questions
- Aspiring Clinical Research Associates (CRAs)
- Life sciences and pharmacy graduates entering clinical research
- Clinical Trial Coordinators (CTCs) and Site Staff
- Professionals transitioning from healthcare, QA, or regulatory roles
- Junior CRAs seeking a structured refresher of core concepts
Upon completion, learners will have the foundational knowledge and regulatory awareness required to support clinical trial monitoring, documentation, and compliance activities in global clinical research environments.
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