Are you supporting a clinical team, responsible for filing and/or other administrative tasks? This 2-day course will guide you through your responsibilities (GCP and others) and shows you how to document, record, file and archive trial material.
Clinical Trial Assistants (CTAs) have a crucial role to play in the clinical research process. They must adequately maintain all the project’s documentation, records and files and archive them according to stringent standards. In addition, Clinical Trial Assistants also assist with periodical reviews of the clinical project records for accuracy and completeness in order to remain audit-ready. Personnel entering clinical research for the first time and having less than one year’s experience have a great need for information and assistance in order to perform this function.
This two-day course covers the basics and regulatory principles that underpin clinical research and also provides a practical coverage of the day to day functions. Theory and interactive exercise make this training the ideal foundation for a career as a CTA.
“Trainer Marleen Verbeeck was speaks very fluid and understandable English. She has a great tempo, is open to questions, is very comfortable with teaching / the topics. She makes the training really pleasant”.
“I would like to thank you for the very helpful and informative CTA training. The content and the organisation were of high quality and I am happy I had the opportunity to participate. Also, I am really grateful for your assistance prior to the course!
Kyriaki Tsigkari - Greece
Shire Hellas Greece
I would like to thank you for the very helpful and informative CTA training. The content and the organisation were of high quality and I am happy I had the opportunity to participate. Also, I am really grateful for your assistance in getting to the training centre this morning! It was very kind of you! I hope that we will have the chance to meet and work together again in the future." (Kyriaki Tsigkari, Medical Affairs Specialist
Tailored Project - Belgium
“The course is very complete and very well explained”.
“Trainer Marleen Verbeeck had a good interaction with the audience. She asks for opinion and own experiences…"
The course gave me an excellent overview of Safety and Serious Adverse Events (SAE) procedures.
Roberta Manfroni
Grunenthal Italia
I want to thank sincerely the ECCRT for the excellent quality of the training provided. I felt warmly welcomed and I was given a very good assistance in organizing the trip, especially thanks to the support of Ms. Veerle Bultinck.
A great thanks to my highly qualified trainer for the clear explanations, for the availability to give us all the clarifications we needed, for the material provided and for the way she managed to motivate us.
I really enjoyed the training, the organization and all the staff!
The course was even better than my expectations!
Sylviane Hauser
Edwards Lifesciences BVBA
It was a very complete course full of good tips and tricks. As I'm new in the job, I did not really know what to expect but I realised that I already do a lot of what Marleen covered. But thanks to Marleen, all the pieces of the puzzle fell into place. Moreover, the course was very interactive with a lot of practical examples from Marleen which is definitely a plus.