Clinical Research Coordinator

Singapore National Eye Centre; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading health institution in Singapore is seeking a Clinical Research Coordinator to manage and coordinate clinical trial activities. The successful candidate will support the Principal Investigator by handling patient recruitment, monitoring, data collection, and compliance with regulatory standards. Ideal applicants will have a degree in Life Sciences, Nursing, or related fields and possess strong time-management and multitasking skills in a collaborative environment. This is an excellent opportunity to contribute to impactful health research.

Qualifications

• Degree in Life Sciences, Nursing, Biomedical Science, or Biological Sciences.
• 1-2 years of related experience preferred.
• Strong time-management and multitasking capabilities needed.
• Ability to work independently and in a team.
• Must be conscientious, meticulous, and self-motivated.

Responsibilities

• Coordinate clinical trial activities according to study protocols.
• Support the Principal Investigator in trial activities.
• Manage patient screening, recruitment, and follow-ups.
• Collect and manage data, resolving discrepancies.
• Organize the collection of biological specimens.
• Monitor adverse events and report safety issues.
• Maintain and organize site files and submissions to ethics committees.
• Track expenditures and ensure timely invoicing.

Skills

Time-management

Multi-tasking

Independent work

Team collaboration

Attention to detail

Education

Degree in Life Sciences/Nursing/Biomedical Science/Biological Sciences

Job description

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National Cancer Centre of Singapore Pte Ltd

Clinical Research Coordinator

Job Category: Research

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