DUBLIN–(BUSINESS WIRE)–The “Live: CRA Beginners F2F Course” training has been added to ResearchAndMarkets.com’s offering.
A 3-day CPD accredited intensive course for those looking to improve their clinical research associate skills (CRA). This course provides a comprehensive and valuable insight into a CRA’s entry-level role. how will I benefit from taking this course?
By the end of this course you will:
- Identify suitable investigators to participate in a clinical trial
- Perform pre-selection visits to assess the suitability of a site to conduct the trial
- Understand what essential study documentations are required to start a trial
- Conduct pre-trial activities including drug (IP) release procedures
- Conduct an initiation visit
- Monitor the conduct at the investigational 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
A “practical” and “hands-on” workshop that focuses on current practice. And the CRA’s role and responsibilities in the context of the regulations and rules governing clinical trials.
We will look at a day in a CRA’s life to provide insight into the profession. Mock-up sample protocols and study documents will be used throughout the course to reinforce the learning. 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 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.
“Excellent course. Better than expected. Discussions and workshops insightful. Course content quite intense, but simplified by excellent instructors. I gained invaluable knowledge of the role of a CRA”
Key Topics Covered:
- 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
For more information about this training visit https://www.researchandmarkets.com/r/rs4f87
Contacts
ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
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