This course is meant to provide clinical research staff with the foundational skills needed to successfully and confidently operationalize clinical research studies. There are thirteen modules that provide clinical research staff with tips and skills on how to review a protocol, conduct informed consent and manage finances and resources, among other topics. We suggest learners review the course on Biomedical Research Ethics which provides an excellent background on research ethics involving human participants, prior to completing this module.
WHO SHOULD TAKE THIS COURSE?
The course may be useful for onboarding new CRCs and other clinical research staff (including new investigators) and is suitable for all clinical research staff conducting clinical research studies in Canada.