The Essentials of Clinical Trials for Investigators
Enhance your readiness as a clinical trial investigator and navigate trial activities with confidence through a flexible learning experience designed to fit your schedule

Course Details
Course Intakes | Registration Periods |
|---|---|
January | 1 December to 24 December |
March | 1 February to 25 February |
June | 1 May to 25 May |
September | 1 August to 25 August |
Course Duration | |
16 weeks (starting from the date of confirmation of registration) | |

Course Description
This is a 16-week online self-paced course that will equip a clinician investigator with the essential skills in navigating through the clinical trial activities with confidence and ease.
The course covers the fundamental operational knowledge of conducting a clinical trial, which includes how to get ahead of administrative tasks with ease, understand the regulatory landscape and what it takes during screening and recruitment. With this knowledge, you can design and optimize the protocol to improve the trial design, management, and/or processes with the highest likelihood of success.
This course can be accessed anytime, anywhere at own pace.
Learning Outcome
Understand the roles and responsibilities of investigators in the conduct and oversight of clinical trials
Understand the ethical requirements and importance of informed consent when recruiting participants
Ensure appropriate medical oversight of participants, including follow-up visits and safety reporting for adverse events
Oversee and manage study team members to ensure they are suitably qualified, trained, and delegated to perform study-related activities
Maintain accurate, complete, and compliant study documentation, including source documents and essential records
Ensure the quality and integrity of study data through proper data collection practices and adherence to regulatory requirements
Who Should Attend
Aspiring clinicians or scientists with interest in clinical trials
Course Outline
Kindly note that the course outline may be subjected to changes without prior notice.
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Note
Participants will be given access to the e-learning materials upon enrolment into the course.
Participants are required to complete all e-learning modules and quizzes by the end of their respective programme intakes.
Application Procedure
Please complete and submit your registration form before the respective intake deadlines.
Registration Form
Please click the link below to access our registration form.
Course Fees (Inclusive of GST)
$350
Qualification
Participants who have completed all eLearning modules will obtain a Certificate of Completion (Essentials of Clinical Trials for Investigators) from SCRI Academy.
To download the programme brochure, please click here (opens in new tab).
Enquiries
If you have any questions or would like to arrange bulk registration for your colleagues or friends, please contact us at scriacademy@scri.cris.sg for more information.
