Clinical Research Coordinator (Heamatology Trials)

Singapore National Eye Centre; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to support investigator-initiated clinical trials. This role involves ensuring compliance with protocols and regulatory requirements while fostering collaboration across teams. The ideal candidate will have a degree in a relevant field and experience in clinical trials, particularly in Hematology/Oncology. Join a dynamic environment where your organizational skills and proactive approach will contribute to impactful research outcomes. If you are passionate about advancing clinical research and enjoy working in a collaborative setting, this opportunity is perfect for you.

Qualifications

• 1-2 years experience in clinical trials, especially in Heamatology/Oncology.
• Knowledge of setting up cell therapy trials and trained in ICH GCP.

Responsibilities

• Achieve study enrollment targets through effective recruitment strategies.
• Collaborate with study teams for subject screening and recruitment.

Skills

Good Clinical Practice (GCP)

Communication Skills

Organizational Skills

Interpersonal Skills

Time Management

Independent Learning

Team Collaboration

Education

Degree in Nursing

Degree in Medicine

Degree in Pharmacy

Degree in Healthcare/Biological Sciences

Job description

National Cancer Centre of Singapore Pte Ltd

Clinical Research Coordinator (Heamatology Trials)

Job Category: Research

Posting Date: 25 Mar 2025

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:

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

Key Requirements:

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