Organization of Clinical Trials and Clinical Monitoring Plan Development
This course introduces the student to elements involved in implementing and managing a clinical trial from the perspective of the research site staff/team. Topics include the identification and evaluation of sites and investigators, on-site budget management, and the coordination of subject participation. Upon completion, students should be able to demonstrate the principles and practices of effective research site management.
Upon completion of this course, the student will learn about coordinating clinical research project, applying regulator, legal, and governing parameters within a clinical research project, Plan and prepare research budgets and contracts, and Recruit, enroll, and retain study subjects.
This course is intended primarily for students wishing to pursue a career in the pharmaceutical industry, in Clinical Research, Drug Safety, and Pharmacovigilance.
In Class Registration CAD$890 +HST | Online Education Registration CAD$525 +HST