The Intermediate – A CRC’s Guide to Clinical Trials and Clinical Research Management

Overview

An intermediate course that equips Clinical Research Coordinators I and Senior Clinical Research Coordinators (CRCs) with the necessary competencies and skills to manage and plan both clinical trials and clinical research activities.

This course is delivered in 3 parts. Firstly, the eLearning portion will guide participants on the necessary know-hows of planning and managing an Investigator Initiated Trial (IIT), as well as management of Investigational Products.

Next, the lectures during the face-to-face workshop will allow participants to gain insights on basic leadership, project management in Clinical Trials and study budgeting skills. The workshop will also include interactive small group discussions on real case scenarios and sharing of best practices.

Finally, participants will then be required to complete an online quiz comprising of Short Answered Questions (SAQs) before concluding with the course.

This course is part of the cluster CRC training series brought to you by SingHealth Clinical Trials Coordinating Centre (CTCC).

Programme Outline*

This course will be delivered in 3 parts:

Part 1 - eLearning Modules

Protocol Design for an Investigator Initiated Trial (IIT)
CRF Design for an IIT
Randomization for an IIT
Re-packaging & Re-labelling of Investigational Products

Part 2 - Face-to-Face Workshop (on 28 Oct 2024)

Project Management in Clinical Trials
Study Budgeting
Time Management and Working with Difficult People (TBC)
Case Studies Discussion

Part 3 - Quiz

The quiz consists of Short Answer Questions (SAQs) based on real case scenarios. Participants will be given 2 weeks to complete the SAQs before submitting their answers via email.

Participants are required to complete Part 1 and Part 2 before they can proceed to attempt the quiz.

*Programme may be subjected to change

Note: Attendance will be taken for all components and an eCertificate of Attendance will be issued after completion of the course.

Target Audience

Clinical Research Coordinators with at least 4 years of experience in the conduct of clinical trials or clinical research studies:

Clinical Research Coordinator I
Senior Clinical Research Coordinator

Dates

Part 1 - eLearning: 30 Sept to 27 Oct 2024 (1 month)
Part 2 - Face-to-Face Workshop: 28 Oct 2024 (1 half-day)
Part 3 - Online Quiz: 29 Oct to 12 Nov 2024 (2 weeks)

Time

Part 2 - Face-to-Face Workshop: 9.00am to 1.00pm
Registration starts from 8.30am

Note: Participants are advised not to schedule appointments/ meetings within the duration of the workshop.

Course Fees

S$870.91* (waived for all SingHealth Clinical Research Coordinators and Research Coordinators i.e. staff mapped to the CRC CDP)

S$1,045.31*(Non-SingHealth staff)

*Inclusive of GST

Note: For SingHealth staff, full course fees will be charged to your department if you do not attend the course

Class Size

30 pax

Venue

SingHealth Academia

Organiser

SingHealth Academy & Clinical Trial Coordinating Centre

Registration Details

NOTE: Please inform and attain approval from your supervisor and respective institution HRs before sending in your registration.

To register, please email the following information to ask@singhealthacademy.edu.sg -
Full name:
Contact number:
Designation:
Department
Institution:
Email address:
Mode of payment (not required for SingHealth CRC/RC): Cheque/ Sponsored by Department/ CT Voucher
Supervisor's name:
Supervisor's designation:
Supervisor's email address:

Number of years of CRC experience:

Nature of research involved (apportion percentage if you are involved in >1 type of research):

S/N	Involvement	Weightage (%)
1	Clinical trials (interventional studies involving drug/biologics, medical device or procedures)
2	Clinical Research (non-interventional studies)
3	Medical Records Review (non-interventional and non-invasive)
4	Questionnaire/Survey/Interview (non-interventional and non-invasive)
5	Others (Please list):
Total		100

Example:

S/N	Involvement	Weightage (%)
1	Clinical trials (interventional studies involving drug/biologics, medical device or procedures)	20
2	Clinical Research (non-interventional studies)	30
3	Medical Records Review (non-interventional and non-invasive)	50
4	Questionnaire/Survey/Interview (non-interventional and non-invasive)	0
5	Others (Please list):
Total		100

Please register by 23 September 2024.

Registration is on a first-come, first-served basis. Successful registrants will be notified via email with information on payment details and instructions for completing the course.

In line with the Singapore Personal Data Protection Act (PDPA), please note that we have updated our SingHealth Data Protection Policy, a copy of which is available at http://www.singhealth.com.sg/pdpa. Hard copies are also available on request.

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