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Clinical Research Associate (CRA) Beginners

Classroom based CPD accredited Clinical Trial Training

Provided by CGX Training

Summary

Price
£2,000 inc VAT
Or £166.67/mo. for 12 months...
Finance options

Easy payment terms are available on request.

Study method
Classroom
Duration
3 days · Part-time
Qualification
No formal qualification
CPD
18 CPD hours / points
Certificates
  • Certificate of completion - Free
Additional info
  • Exam(s) / assessment(s) is included in price
  • Tutor is available to students

Location & dates

Location
Start date
End date
14/07/2025
16/07/2025

End date: 16/07/2025

Additional info: Duration 09:30am - 16:30pm each day and lunch is provided.

Address
Citadines Holborn
High Holborn
Central London
London
WC1V6LF
United Kingdom
27/10/2025
29/10/2025

End date: 29/10/2025

Additional info: Duration 09:30am - 16:30pm each day and lunch is provided.

Address
Citadines Holborn
High Holborn
Central London
London
WC1V6LF
United Kingdom

Overview

A clinical Research Associate (CRA) primarily manages the managerial aspects of a number of clinical trials, at every stage of the process.

If you are a clinical trial administrator who has just been promoted to a CRA level I or have limited experience as a CRA this modular training is specifically designed for you. You may be a research nurse or a former data manager who has landed their first role as a CRA. This is a good starter course that will equip you with the skills to conduct clinical trial initiation and or/ monitoring and basic site management at the investigational site.

Certificates

Certificate of completion

Digital certificate - Included

CPD

18 CPD hours / points
Accredited by The CPD Certification Service

Course media

Resources

  • CRA Beginners Course -

Description

This is fundamentally a “practical” and “hands on” workshop that focuses on current practice to ensure the CRA delegate develops practical experience of the role. Participants will learn about the role and responsibilities of the clinical research associate in the context of the regulations and rules that govern clinical trials. Practical session demonstrating real life setting as well as case scenarios will be adopted. A look at the ‘day in the life of a CRA’ will provide further insight into the profession. Mock up sample protocols, and study documents will be reviewed and practically used throughout the course to reinforce the learning concepts.

CLINICAL RESEARCH ASSOCIATE (CRA)

Are you a CTA looking to advance to a CRA level? Are you a CRA with limited experience seeking training to improve your skills and performance? Are you a Research Nurse or Data Manager who has landed your first CRA role? If so, this Clinical Research Associate course provided by CGX Training is an excellent starter course that can equip you with the skills to conduct clinical trial initiation and or/ monitoring and basic site management at the investigator site.

A CPD accredited 3-day intensive course which provides those starting or looking to improve their skills as a CRA with a comprehensive and valuable insight into the entry-level role of a Clinical Research Associate (CRA).

A clinical Research Associate (CRA) primarily manages the managerial aspects of a number of clinical trials, at every stage of the process.

This is fundamentally a “practical” and “hands on” workshop that focuses on current practice to ensure the CRA delegate develops practical experience of the role. Participants will learn about the role and responsibilities of the clinical research associate in the context of the regulations and rules that govern clinical trials.

TOPICS

  • ICH- GCP
  • The primary duties of a CRA
  • The specific responsibilities in accordance with ICH-GCP, SOP and regulations:
  • Before the clinical phase of the trial commences
  • During the clinical conduct of the trial
  • After completion or termination of the trial
  • Essential documents- Preparation, collation and QC
  • Ethics and regulatory submissions and approvals of the clinical trial application
  • Study Start up activities- site identification and selection, QC for IP release
  • Site Activation- SIV, ISF review and Drug supply review
  • Monitoring and Site Management
  • Study site close out activities

Who is this course for?

Who is the course Designed For?

If you are a clinical trial administrator who has just been promoted to a CRA level I or have limited experience as a CRA this this modular training is specifically designed for you. You may be a research nurse or a former data manager who has landed their first role as a CRA. This is a good starter course that will equip you with the skills to conduct clinical trial initiation and or/ monitoring and basic site management at the investigator site.

How will I benefit from taking this course?

  • Identify suitable Investigator for participate in a clinical trial.
  • Perform pre-selection visits to assess the suitability of a site to conduct the trial.
  • Understanding of what essential study documentation necessary are required start a trial
  • Conduct Pre-trial procedures including drug release IP
  • set up Investigator sites for conduct of the study
  • Conduct an initiation visit
  • Monitor the conduct at the investigator site
  • Review source documentation and site file review
  • Perform site management activities
  • Conduct a close-out visit at the end of the study.
  • Complete a clinical trial

Requirements

Minimum entry requirements: 5 GCSE passes one in a science subject.

Career path

CPM - Clinical Project Manager

Questions and answers

Reviews

Currently there are no reviews for this course. Be the first to leave a review.

Provider

CGX Training

About CGX Training

CGX Training is a clinical trial specialist training provider offering both traditional and e-learning courses to

Clinical Trial Professionals (CTPs). We service corporate, healthcare companies and individual trainees seeking

to embark on a career in this industry, and those requiring Continuous Professional Development (CPD). As a

member of the CPD Certification Service, our accredited courses, training and workshops qualify for CPD.

 

Dedicated to raising professionalism and standards in clinical trial management

CGX’s tailored training solutions provide end-to-end learning and development programmes for organisations

of all sizes and individuals embarking on a career in the Clinical Trial sector. We are involved in every aspect,

from identifying skills gaps to delivering practical training courses and provision of internationally recognised

qualifications. Our bespoke programmes are designed to improve marketing capability and build business advantage.

CGX delivers clinical research education to schools, colleges and universities, to promote career opportunities in clinical

trials as part of its commitment to promote STEM (Science, Technology, Engineering and Mathematics) education and

broaden career options for young adults.

CGX also offers consultancy services to the clinical research industry to ensure the safety, quality and cost-efficiency of

clinical trials. We deliver practical and interactive training courses using a variety of methodologies and tools.

 

Example Training Courses/Modules

Clinical Trial Associate (CTA) Entry level / Intermediate

Clinical Research Associate (CRA) Entry level / Intermediate

Clinical Trial Manager (CPM) Entry level / Intermediate

Auditing in Clinical Trials

Good Clinical Practice (GCP) and Inspection Readiness

Risk-Based Monitoring

Soft Skills Training for the Clinical Trial Professionals

 

Customer Testimonial

Adrian: "My first contact with CGX training was a phone call to enquire about the course - CTA for beginners. I knew that I wanted to begin a career in the pharmaceutical industry but had heard that getting started can be difficult. I was really grateful to Donnamarie who took my call and kindly spent near on an hour answering my various questions and helping me to better understand the career pathway and what jobs I should be applying for. This advice was given even before I had signed up to the course. After taking the course, I found the course very useful. The hands on workshops were excellent, as well as the excellent teaching. The course tutor, Donnamarie very clearly cared a lot about teaching us well. I am certain it will help me get that extra advantage over other applicants."

View CGX Training profile

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