DUBLIN–(BUSINESS WIRE)–The “CTA Beginners F2F Course” training has been added to ResearchAndMarkets.com’s offering.
This CPD accredited 3-day intensive course is for those looking to enter the field of Clinical Research. It provides a comprehensive insight for an entry-level Clinical Trial Administrator (CTA) role.
This fundamental “”how-to”” and “”why”” course focuses on introducing the participant to the clinical processes, to facilitate successful entry into the clinical trial industry. Participants will learn about the clinical trial administrator’s role and responsibilities in the context of the regulations and rules that govern clinical trials.
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. 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 insight into the clinical trial process, terminology and can show you how to enter the clinical trial industry.
How will I benefit from taking this course?
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
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/fljrd4
Contacts
ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
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