Clinical Research Course for Investigators/Sponsor-Investigators
This course was designed by two highly experienced clinical research professionals (both with combined roles of senior auditor, clinical study manager, site study coordinator/nurse, senior monitor) to give new or aspiring investigators (or even those wanting a 'refresher’) concise and relevant knowledge for this very important role. It can also be offered to investigators who following a health authority inspection, had an observation of inadequate Investigator oversight.
By the end of this course, the Investigator will understand his/her role and responsibilities (and those of his/her team) in the conduct of a clinical study; delegation of tasks; protocol compliance; regulatory and ethical expectations; source and essential documents; safety reporting; visits from monitors, auditors and inspectors; and the dual role of sponsor-investigator.
This 2.5-hour training can be conducted onsite or remotely via Teams.
Offered in English and in French.
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