DUBLIN–(BUSINESS WIRE)–The “CRA Beginners Online Course” training has been added to ResearchAndMarkets.com’s offering.
A CPD accredited 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). 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 clinical Research Associate (CRA) primarily manages the managerial aspects of a number of clinical trials, at every stage of the process. 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.
Key Topics Covered:
- 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
For more information about this training visit https://www.researchandmarkets.com/r/e07dgx
Contacts
ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
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