This is a 16-week introductory eLearning programme for aspiring individuals with an interest in clinical trials.
Course Description & Learning Outcomes
At the end of the course, you will be able to: 1) Describe the various key activities involved in conducting clinical trials at site. 2) Understand the different roles and responsibilities of the study team members and the various stakeholders. 3) Read and understand a study protocol. 4) Conduct study start up activities, informed consent process, screening, recruitment and follow up of participants. 5) Report safety events in accordance with the IRB requirements. 6) Understand the trial closure process.
Date: 01 Jan 2024, Monday
Time: 12:00 AM - 12:00 AM (GMT +8:00) Kuala Lumpur, Singapore
Course fees: SGD350 (inclusive of GST)