The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials while working very closely with the Investigator. The CRC will develop, implement, and coordinate research and administrative procedures for the successful completion of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols.

Source adaptation: https://www.sokanu.com/careers/clinical-research-coordinator/

NUHS IMU CRC-Investigator Workshop 2024

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IMU Learning Series

 

Date Topic Speaker Venue
January 22
2 to 3pm		 How can CRCs facilitate a clinical trial Stephanie Tan
(IMU)		 MD6 Seminar Room #09-01T
March 11
10 to 11am		 Roles of a Clinical Project Manager in a Project Lifecycle Joanna Chang
(IMU)		 MD6 Seminar Room #08-01T
April 8
10 to 11am		 The Similarities and Differences between Drug and Device Trials Geraldine Seow
(Johnson & Johnson)		 MD6 Seminar Room #08-01T
May 13
10 to 11am		 Data Management Chan Peng
(Tech Observer)		 MD6 Seminar Room #08-01T
June 10
10 to 11am		 Monitoring 101 Lim Xiao Jing
(Syneoshealth)		 MD6 Seminar Room #08-01T
July 8
10 to 11am		 Contracts 101 Nick Ho
(IQVIA)		 MD6 Seminar Room #08-01T
August 5
10 to 11am		 Marissa See
(Bayer)		 MD6 Seminar Room #08-01T
August 26
10 to 11am		 Proposal Development Jessica Lee
(IMU)		 MD6 Seminar Room #08-01T
September 16
10 to 11am		 Emotional Intelligence Srinivas
(IQVIA)		 MD6 Seminar Room #08-01T
October 14
10 to 11am		 Common Audit and Inspection Findings Chua Wei Ting
(Syneoshealth)		 MD6 Seminar Room #08-01T
November 11
10 to 11am		 The Common Difficulties / Difficulties Faced with Trial Set-up
(The Most Memorable Experience of Speaker)		 Chan Lilian
(IQVIA)		 MD6 Seminar Room #08-01T

 

Date Topic Speaker Company
November 12, 2018 How do the research team of the pharma decide which drug needs Post Marketing Study (PMS)? Bernard Ng Bayer
October 15, 2018 Clinical Trial Monitoring and Informed Consent in Vulnerable Subjects (Updates) Chua Wei Ting Syneos Health
September 24, 2018 8 steps to Influence Others Srinivas IQVIA
September 10, 2018 Common Audit and Inspection Findings Michelle Ho Syneos Health
August 27, 2018 The Similarities and Differences between Early and Mid-late Phase Studies?
What are the lessons learnt and what are the pitfalls of early phase studies?		 Chong Chew Lan Celerion
August 13, 2018 The Common Difficulties / Difficulties faced with Trial Set-up
(The Most Memorable Experience of Speaker)		 Chan Lilian IQVIA
June 18, 2018 Understanding the Medtech Industry Alok Mishra Value Addition
May 21, 2018 The Similarities and Differences between Drug and Device Trials Geraldine Seow Johnson & Johnson
April 09, 2018 The Pros and Cons of the Increasing Needs for Remote Monitoring. Nelson Wong CSI Medical Research
March 12, 2018 Regulatory Requirements for Clinical Trials
(Investigator Initiated Trials and Industry Sponsored Trials)		 Lim Xiao Jing Syneos Health
January 15, 2018 Contracts between Sponsor and Site Nick Ho IQVIA
November 13, 2017 Clinical Trial Monitoring and Informed Consent in Vulnerable Subjects Chua Wei Ting INC Research
October 16, 2017 Updates to ICH GCP and Inspection Readiness Michelle Ho INC Research
September 11, 2017 C2C- My Journey from Coordinator to CRA Nelson Wong Quintiles
August 14, 2017 Expedited Safety Reporting Requirements and Notification of Serious Breach in Clinical Trials Lim Xiao Jing INC Research
July 24, 2017 Taking Part in a Global Clinical Trial – How does my site get chosen, and How do I decide if this trial is right for me Adeline Sng Quintiles
July 10, 2017 Differences and Similarities between Working at an Academic/Research Institution and Industry (Pharma/CRO) Dr Foo Chuan Kit Bayer
June 12, 2017 Clinical Trials Management from CRO perspective Chan Lilian
Liang Pei Ling		 Quintiles
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