Clinical Research Associate (CRA) Beginners Online Course
An Online Interactive course CPD accredited Clinical Trial Training
CGX Training
Summary
Easy payment terms are available on request.
- Certificate of completion - Free
- Exam(s) / assessment(s) is included in price
- Tutor is available to students
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Dates
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
Course media
Resources
- CRA Beginners Course -
Description
This is a course that focuses on current clinical practises to ensure the delegate develops a thorough insight on the role of a CRA. 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. There will be discussions concerning real life settings 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. There will be an assessment at the end of the 3 weeks with a pass mark of 70%
CRA CLINICAL RESEARCH ASSOCIATE
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-week, part-time 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 investigational 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
CRA - Clinical Research Associate
CPM - Clinical Project Manager
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Legal information
This course is advertised on reed.co.uk by the Course Provider, whose terms and conditions apply. Purchases are made directly from the Course Provider, and as such, content and materials are supplied by the Course Provider directly. Reed is acting as agent and not reseller in relation to this course. Reed's only responsibility is to facilitate your payment for the course. It is your responsibility to review and agree to the Course Provider's terms and conditions and satisfy yourself as to the suitability of the course you intend to purchase. Reed will not have any responsibility for the content of the course and/or associated materials.