DUBLIN–(BUSINESS WIRE)–The “CTA Beginners Online Course” training has been added to ResearchAndMarkets.com’s offering.
The facilitator will take you through case scenarios and simulation exercises and discuss a marketed product’s life cycle. Sample trial master files and study documents will be reviewed and constructed to reinforce the learning concepts.
The online courses take place in virtual classrooms and are instructor-led by a course trainer. The courses will run using our CGX online Learning Management System (LMS).
By the end of this course you will:
- Understand the stages and phases involved in clinical trial development
- Understand the life cycle of a clinical trial
- Understand why clinical trials are needed
- Understand who regulates clinical trials and what are the rules, regulations (GCP)
- Understand who the key professionals involved in clinical research are
- Understand where the CTA role and responsibilities fit in
- Understand some key terminology and acronyms
- Identify the key safeguards required to ensure patient safety and well being
- Be able to identify the key safeguards required to ensure data quality standards are met
- Understand what is a Trial Master file and the key documentation that make up the file
The CPD Accredited CTA Online Interactive Version of the course is conducted 2 days a week. Running at 3 hours each day over the course of 3 weeks. Around 18 training hours in total. Training takes place on Mondays and Tuesdays, and commences at 09:30hrs. Who is the course designed for?
If you are new to clinical research or an administrator who has just started working in clinical trials (entry level CTAs) this module is specifically designed for you.
Alternatively, you may be a graduate who has just left university wishing to pursue a career in clinical trials. This is a good starter course that will equip you with the insight into the clinical trial process, terminology and can show you how to enter the clinical trial industry.
Key Topics Covered:
- What is a clinical trial
- The four clinical trial stages
- Exploring the necessity for clinical trials
- The key personnel involved in clinical trials safeguarding subjects participation
- The rules and regulations governing clinical trials (ICH-GCP)
- The overall process for a clinical trial
- The role of the clinical trial administrator in the context of a clinical trial
- Review the documents required for a clinical trial and the master file i.e. TMF
For more information about this training visit https://www.researchandmarkets.com/r/is8j5i
Contacts
ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
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