Clinical Research Associate (CRA) Training

CRA TRAINING COURSE INFORMATION

£349

Develop a practical understanding of the Clinical Research Associate role and the knowledge required to support the effective monitoring and oversight of clinical trials.

Created by clinical research professionals with more than 35 years of international industry experience, this online Clinical Research Associate training course explains how clinical trials progress from study start-up through to closeout, and how CRAs help protect participants, maintain compliance and support reliable clinical trial data.

The course is suitable for aspiring and newly appointed CRAs, clinical research professionals looking to expand their knowledge and organisations requiring consistent CRA training across their teams.

Current Status

Price

£349.00

Get Started

Take this Course

Download Course Leaflet

KEY FEATURES OF OUR ONLINE CLINICAL RESEARCH ASSOCIATE TRAINING COURSE:

100% online and available on demand
Learn anywhere, at your own pace
Developed by experts with more than 35 years of clinical research experience
Comprehensive introduction to the role and responsibilities of a CRA
Covers clinical trial activities from study start-up to closeout
Includes Good Clinical Practice and Good Documentation Practice
Practical guidance on site monitoring and essential records
Interactive content, realistic examples and robust knowledge checks
Certificate awarded upon successful completion
Suitable for individual learners and corporate teams

Course Content

Course Navigation

Course Support

PRACTICAL CRA TRAINING DEVELOPED BY CLINICAL RESEARCH EXPERTS

Clinical Research Associates play an important role in helping clinical trials operate safely, ethically and in accordance with the study protocol, Good Clinical Practice and applicable regulatory requirements.

Working on behalf of a sponsor or Contract Research Organisation, a CRA may support site selection, site initiation, routine monitoring and study closeout. The role involves communicating with investigators and site teams, reviewing clinical trial records, identifying potential compliance issues and confirming that participant rights, safety and wellbeing remain protected.

Our online Clinical Research Associate training course provides a structured introduction to these responsibilities and the wider clinical trial environment in which CRAs work.

You will explore the complete clinical trial lifecycle, including study start-up, site selection, site initiation, monitoring activities, protocol compliance, participant safety, source documentation, data quality, essential records and study closeout.

The course also explains the principles of Good Clinical Practice and Good Documentation Practice, helping learners understand why complete, accurate and traceable clinical trial records are essential for regulatory compliance and reliable research results.

Rather than simply presenting theoretical information, the training uses practical explanations, realistic clinical research examples, interactive content and knowledge checks to demonstrate how CRA responsibilities are applied in real situations.

This course can help learners build relevant clinical research knowledge and prepare for CRA responsibilities. Completion does not guarantee employment or replace the role-specific experience, employer training or qualifications that individual organisations may require.

CLINICAL RESEARCH ASSOCIATE TRAINING FOR INDIVIDUALS AND TEAMS

INDIVIDUAL LEARNERS

Individual professionals gain immediate online access and can complete the CRA training at a time, location and pace that suits you.

START THE CRA TRAINING COURSE NOW

CORPORATE TEAMS

Our multiple licence options help you provide consistent training across your teams while improving training and simplifying course administration and training oversight.

REQUEST CORPORATE TRAINING INFORMATION

Get certified. Stay compliant. Advance your career.

Join thousands of professionals who have completed our training.

WHAT WILL I LEARN FROM THIS CRA TRAINING COURSE?

Gain proficiency in managing clinical trials from study start-up to closeout, including protocol development, site selection, and monitoring.

Understand and apply GCP and GDocP standards to ensure adherence to regulatory requirements and maintain data integrity.

Learn to perform effective monitoring visits, ensuring compliance with trial protocols and regulatory guidelines.

Master the creation and maintenance of essential clinical trial records, ensuring compliance with regulatory standards.

FAQs

FREQUENTLY ASKED QUESTIONS ABOUT CLINICAL RESEARCH ASSOCIATE TRAINING

WHAT DOES A CLINICAL RESEARCH ASSOCIATE DO?

A Clinical Research Associate monitors and supports clinical trial sites on behalf of a sponsor or Contract Research Organisation.

Responsibilities can include assessing potential trial sites, supporting site initiation, reviewing trial conduct and documentation, monitoring compliance with the protocol and Good Clinical Practice, following up identified issues and supporting study closeout.

The precise responsibilities will depend on the organisation, clinical trial and level of experience.

WHO SHOULD COMPLETE THIS CRA TRAINING COURSE?

The course is suitable for aspiring and newly appointed Clinical Research Associates, as well as people working in related clinical research roles, including:

Clinical Trial Assistants
Clinical Research Coordinators
Study-site personnel
Clinical Trial Managers
Sponsor and CRO employees
Regulatory affairs professionals
Quality assurance and compliance personnel
Medical affairs professionals
People looking to move into clinical trial monitoring

It may also be useful for experienced clinical research professionals who want to refresh or broaden their understanding of CRA responsibilities.

DO I NEED A DEGREE TO TAKE THE CRA COURSE?

No specific degree is required to enrol in this online course.

Employers commonly set their own entry requirements for CRA positions, which may include a relevant scientific, healthcare or clinical research qualification and previous industry experience. Completing this training can strengthen your understanding of the role but does not override an employer’s individual recruitment requirements.

WHAT IS THE DIFFERENCE BETWEEN CRA TRAINING AND GCP TRAINING?

Good Clinical Practice training explains the ethical, scientific and quality principles that apply to clinical trials involving human participants.

CRA training is more role-specific. It explores how Clinical Research Associates support and monitor clinical trials, work with investigation sites, review documentation and follow up compliance issues.

Some employers may require both role-specific CRA training and a current comprehensive GCP course certificate.

WILL THIS COURSE MAKE ME A CERTIFIED CLINICAL RESEARCH ASSOCIATE?

The course provides a certificate of successful completion, but it should not be represented as an independent professional licence or guarantee of employment as a CRA.

Employers may also require relevant qualifications, clinical research experience, current GCP training and organisation-specific competency assessments.

CAN ORGANISATIONS PURCHASE MULTIPLE CRA COURSE LICENCES?

Yes. Corporate and team licences are available for organisations that need to train multiple employees, contractors or clinical research personnel.

Multiple licences can support consistent training while allowing organisations to manage enrolment, learner progress and completion records centrally. Contact us with your approximate number of learners to receive a tailored quotation.

WHAT MAKES INTEGRITY CLINICAL COMPLIANCE’S CRA TRAINING DIFFERENT?

The course is written by experienced clinical research professionals and is designed to support practical understanding rather than tick-box learning.

Interactive content, realistic clinical research examples and robust knowledge checks help learners understand how CRA responsibilities apply across real clinical trial activities.

If this course isn’t right for you, take a look at our other online clinical courses.