Clinical Research Coordinator

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

Select how often (in days) to receive an alert:

National Cancer Centre of Singapore Pte Ltd

Clinical Research Coordinator

Job Category: Research

Posting Date: 10 Sept 2026

As a clinical research coordinator, you will be actively involved in coordinating clinical trial activities according to the study protocol and in compliance to the ICH Good Clinical Practice guidelines and the Health Products (Therapeutic Products) Regulations under the Health Product Act.

You will support and assist the Principal Investigator in the following trial related activities:

• Patient screening and recruitment,
• Monitoring subject’s compliance to their treatment and follow-up,
• Data collection and management including resolving data discrepancies,
• Coordinating the collection of biological specimens,
• Monitoring of adverse events and safety reporting,
• Maintaining and organising of investigator site files, preparation and submissions to the ethics committee and relevant local health authorities,
• Tracking of trial expenditures and timely invoicing.

Requirements:

• Degree in Life Sciences/ Nursing/ Biomedical Science/ Biological Sciences
• 1-2 years of related working experience will be advantageous
• Good time-management and strong ability to multi-task
• Able to work independently and as a team
• Conscientious, meticulous and self-motivated