Clinical Research Coordinator (Heamatology Trials) - NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD

Roles & Responsibilities

The Clinical Research Coordinator (CRC) shall help investigators conduct mainly investigator-initiated clinical trials. The CRC has to ensure that clinical trials are conducted and recorded in accordance with the protocol, Good Clinical Practice (GCP) Guidelines, all applicable regulatory requirements and the Clinical Trials Operations’ Standard Operating Procedures.

Key Responsibilities :

• Accomplish the study’s target enrolment as per agreed study timelines or shorter through effective recruitment strategies.
• Regular discussion or follow-up with study team on subject screening & recruitment rates eg. email communication or team meetings with Drs.
• Timely response / followup to email enquiries within 10 working days or less.
• Foster good working relationships and collaborate effectively across all streams to promote operational efficiency
• Invoicing is carried out on time and payment can be received with minimal delays.

Key Requirements :

Tell employers what skills you have

Hematology

Clinical Research

Clinical Research Administration

Interpersonal Skills

Healthcare

Medicine

Oncology

Invoicing

patient recruitment

Oncology Clinical Research

Clinical Trials

Protocol

Clinical Trial Management

clinical trials protocols

Nursing

Regulatory Requirements

Life Sciences

Screening

Cell Therapy

Trial Management