Overview
Course Code
SCCR240
Instructor
Faiza Khawaja
Credential Earned
Certificate of completion
Course Type
Part-Time
Course Length
12 weeks
Course Delivery
Virtual
Application Method
Self-service Registration
OSAP Eligibility
No
About the Course
Elements of Clinical Study Coordination SCCR240 is part of the Clinical Research Program. This course will provide learners with the advanced level of knowledge and skills needed to coordinate and organize trials at clinical sites. The content will explore the planning and execution of the trial from the site’s perspective, focusing on the varied functions carried out by the study coordinator to ensure a successful trial.
Topics covered include:
- Introduction to Study Coordination
- Financial Management of Clinical Trials
- Site Management
- Source Document Design and Organization
- Pre-screening
- Study Visits
- Interaction with REBs and Sponsors
- Study Close-out
Outcomes
Upon successful completion of the course, learners will be able to:
- Explain the roles and responsibilities of a study coordinator
- Describe the clinical trial budgeting and negotiation processes
- Develop an effective recruitment plan
- Identify the skills necessary to prepare sites to conduct clinical trials
- Describe the steps and procedures involved in effective site management
- Design and organize source documents to meet protocol requirements
- Describe effective methods for communicating with the REB and the sponsor
- Identify steps to manage the final closeout and archive the study