Clinical Research Coordinator - Trial Ops & Compliance

SingHealth Group; Singapore; On-site; SGD 42,000 - 66,000; Full time

Job summary

National Cancer Centre of Singapore Pte Ltd is seeking a Clinical Research Coordinator to actively coordinate clinical trial activities according to the study protocol and in compliance with ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.

You will support the Principal Investigator in patient screening and recruitment, data collection, specimen coordination, adverse event monitoring, ethics submissions, and trial

Qualifications

• Degree in Life Sciences, Nursing, Biomedical Science or Biological Sciences.
• 1–2 years related experience is advantageous.
• Strong time-management and multi-tasking ability.
• Able to work independently and in a team.
• Conscientious, meticulous and self-motivated.

Responsibilities

• Coordinate clinical trial activities according to the study protocol.
• Screen and recruit patients and monitor treatment follow-up.
• Collect and manage data, resolving discrepancies.
• Coordinate collection of biological specimens.
• Monitor adverse events and safety reporting.
• Prepare and submit ethics documents and liaise with health authorities.
• Track trial expenditures and invoicing.

Skills

Time management

Multi-tasking

Independent worker

Team collaboration

Education

Life sciences degree

Job description

National Cancer Centre of Singapore Pte Ltd is seeking a Clinical Research Coordinator to actively coordinate clinical trial activities according to the study protocol and in compliance with ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.

You will support the Principal Investigator in patient screening and recruitment, data collection, specimen coordination, adverse event monitoring, ethics submissions, and trial