Clinical Research Coordinator

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/

Key Responsibilities of a Clinical Research Coordinator

IMU Learning Series

DateTopicSpeakerVenue
January 22
2 to 3pm
How can CRCs facilitate a clinical trialStephanie Tan
(IMU)
MD6 Seminar Room #09-01T
March 11
10 to 11am
Roles of a Clinical Project Manager in a Project LifecycleJoanna Chang
(IMU)
MD6 Seminar Room #08-01T
April 8
10 to 11am
The Similarities and Differences between Drug and Device TrialsGeraldine Seow
(Johnson & Johnson)
MD6 Seminar Room #08-01T
May 13
10 to 11am
Data ManagementChan Peng
(Tech Observer)
MD6 Seminar Room #08-01T
June 10
10 to 11am
Monitoring 101Lim Xiao Jing
(Syneoshealth)
MD6 Seminar Room #08-01T
July 8
10 to 11am
Contracts 101Nick 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 DevelopmentJessica Lee
(IMU)
MD6 Seminar Room #08-01T
September 16
10 to 11am
Emotional IntelligenceSrinivas
(IQVIA)
MD6 Seminar Room #08-01T
October 14
10 to 11am
Common Audit and Inspection FindingsChua 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
DateTopicSpeakerCompany
November 12, 2018How do the research team of the pharma decide which drug needs Post Marketing Study (PMS)?Bernard NgBayer
October 15, 2018Clinical Trial Monitoring and Informed Consent in Vulnerable Subjects (Updates)Chua Wei TingSyneos Health
September 24, 20188 steps to Influence OthersSrinivasIQVIA
September 10, 2018Common Audit and Inspection FindingsMichelle HoSyneos Health
August 27, 2018The 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 LanCelerion
August 13, 2018The Common Difficulties / Difficulties faced with Trial Set-up
(The Most Memorable Experience of Speaker)
Chan LilianIQVIA
June 18, 2018Understanding the Medtech IndustryAlok MishraValue Addition
May 21, 2018The Similarities and Differences between Drug and Device TrialsGeraldine SeowJohnson & Johnson
April 09, 2018The Pros and Cons of the Increasing Needs for Remote Monitoring.Nelson WongCSI Medical Research
March 12, 2018Regulatory Requirements for Clinical Trials
(Investigator Initiated Trials and Industry Sponsored Trials)
Lim Xiao JingSyneos Health
January 15, 2018Contracts between Sponsor and SiteNick HoIQVIA
November 13, 2017Clinical Trial Monitoring and Informed Consent in Vulnerable SubjectsChua Wei Ting
INC Research
October 16, 2017Updates to ICH GCP and Inspection ReadinessMichelle Ho
INC Research
September 11, 2017C2C- My Journey from Coordinator to CRANelson WongQuintiles
August 14, 2017Expedited Safety Reporting Requirements and Notification of Serious Breach in Clinical TrialsLim Xiao Jing
INC Research
July 24, 2017Taking Part in a Global Clinical Trial – How does my site get chosen, and How do I decide if this trial is right for meAdeline Sng
Quintiles
July 10, 2017Differences and Similarities between Working at an Academic/Research Institution and Industry (Pharma/CRO)Dr Foo Chuan Kit
Bayer
June 12, 2017Clinical Trials Management from CRO perspective Chan Lilian
Liang Pei Ling
Quintiles