Clinical Research Coordinator

NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading healthcare institution in Singapore is seeking a Clinical Research Coordinator to oversee clinical trials and ensure compliance with regulations. The role involves coordinating patient recruitment, data collection, and collaborating with the Principal Investigator on various trial activities. Ideal candidates will possess a solid educational background in Life Sciences or Nursing, with strong organizational skills and the ability to work both independently and as part of a team.

Qualifications

• Degree in Life Sciences/Nursing or Diploma in Nursing with 6 years experience.
• 2 years related experience is advantageous.
• Excellent time-management and communication skills.

Responsibilities

• Coordinate clinical trial activities according to study protocol.
• Support Principal Investigator with patient screening and data management.
• Monitor compliance and adverse events reporting.

Skills

Time-management

Communication

Detail-oriented

Teamwork

Self-motivated

MS Office applications

Education

Degree in Life Sciences/Nursing

Diploma in Nursing

Job description

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
• OR Diploma in Nursing with minimum 6 years working experience as CRC
• 2 years of related working experience will be advantageous
• Excellent time-management and communication skills
• Able to work independently and as a team
• Detail-oriented and self-motivated
• Good grasp of MS Office applications