NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD - Clinical Research Coordinator

Roles & Responsibilities

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 :

Tell employers what skills you have

Multi Tasking

Clinical Research

Interpersonal Skills

Treatment

Healthcare

Oncology

Invoicing

Administration

Oncology Clinical Research

Data Entry

MS Office

Clinical Trials

Protocol

Clinical Trial Management

Compliance

clinical trials protocols

Communication Skills

Life Sciences

Screening

Able To Work Independently