Clinical Research Coordinator (Heamatology Trials)

NATIONAL CANCER CENTRE OF SINGAPORE PTE LTD; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A leading healthcare institution in Singapore is seeking a Clinical Research Coordinator to assist in conducting clinical trials. This role requires a degree in a relevant field and 1-2 years of experience in clinical trials, particularly in Haematology/Oncology. The ideal candidate will excel at managing enrolment targets, ensuring compliance with GCP and will be a strong communicator and team player.

Qualifications

• 1-2 years experience in the conduct of clinical trials, specializing in Haematology / Oncology interventional trials.
• Must have knowledge of setting up cell therapy trials.
• Must already been trained in ICH GCP.

Responsibilities

• Ensure clinical trials are conducted in accordance with protocol and GCP guidelines.
• Accomplish study’s target enrollment through effective recruitment strategies.
• Foster good working relationships across teams.

Skills

Good communication and interpersonal skills

Meticulous and possesses good organizational and time management skills

Independent learner

Team player

Proactive in learning

Education

Degree in Nursing, Medicine, Pharmacy or Healthcare

Job description

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:

• Degree in Nursing, Degree in Medicine, Pharmacy or Healthcare / biological sciences, preferably with experience in clinical trials or clinical research.
• 1-2 years experience in the conduct of clinical trials, specializing in Heamatology / Oncology interventional trials, governed under Health Product Act.
• Must have knowledge of setting up cell therapy trials.
• Must already been trained in ICH GCP.
• Meticulous and possesses good organizational and time management skills.
• Good communication and interpersonal skills.
• Independent learner, Meticulous and possesses good organizational and time management skills.
• Team player and work well with external collaborators and partners.
• Proactive in learning and helping other CRCs in issues with trial management