Research Drive offers an unique tailor made CRA training program for starters in the Healthcare industry. The training starts with a theoretical part and introduces the nature and concepts of Clinical Research, the Clinical Trial process and the Regulatory framework in which clinical research is conducted.
Modules cover the ethical, legal and regulatory considerations that affect clinical trials, the essentials of Good Clinical Practice, the design and conduct of the clinical protocol, biostatistics, data management, and product development. The participant will learn the role & responsibilities of the CRA, Study Site Staff and Sponsor. Participants develop a thorough knowledge base of the European Clinical Trial Directive, FDA Regulations (Code of Federal Regulations Title 21) and the International ICH Guidelines and Good Clinical Practice-GCP.
For more information, please send an email to firstname.lastname@example.org.