Research Coordinator

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

Job summary

An established industry player in healthcare is seeking a Research Coordinator to join their team. This role involves coordinating clinical trials and research studies, assisting investigators with patient recruitment, and managing data collection. The ideal candidate will have a degree in Health Sciences or a Diploma in Nursing, with strong communication and interpersonal skills. By joining this dynamic organization, you will contribute to groundbreaking research aimed at improving cancer outcomes and providing hope for patients. If you are passionate about making a difference in the field of oncology, this is an exciting opportunity for you.

Qualifications

• 2 years of experience in clinical trials is preferred.
• Training in Good Clinical Practice is an advantage.

Responsibilities

• Coordinate oncology-related clinical trials and research studies.
• Assist with ethical/regulatory submissions and patient recruitment.
• Manage data collection and ensure proper filing of research documents.

Skills

Communication Skills

Interpersonal Skills

Time Management

Ability to Multi-task

Education

Degree in Health Sciences

Diploma in Nursing

Job description

National Cancer Centre of Singapore Pte Ltd

Research Coordinator

Job Category: Allied Health Professional

Posting Date: 29 Mar 2025

About Us

The National Cancer Centre Singapore (NCCS) is a leading national and regional tertiary cancer centre, attending to the majority of cancer cases in Singapore’s public healthcare sector. We offer world-class oncology care by having the best talent, doing robust clinical and translational research, and leading education efforts to improve cancer outcomes. Join us to build a meaningful career and offer patients hope for a cancer-free tomorrow.

About the Role

You will be involved in coordinating oncology-related clinical trials and research studies and assist the Investigators with patient recruitment, monitoring of treatment and follow-up, collecting data and tissue specimens (if applicable), and data management.

Key Responsibilities

1. Assist with ethical/regulatory submissions and renewal
2. Coordinate clinical research studies/trials (screening, recruitment, follow-up) and blood/tissue specimens collection if applicable
3. Data collection and management
4. Ensure all research documents are filed accordingly
5. Assist and prepare for monitoring/audit
6. Keep track of research finance budget
7. Maintain laboratory supplies and ensure proper collection, handling, and shipment delivery if applicable

Job Requirements

1. Degree in Health Sciences or Diploma in Nursing
2. 2 years working experience
3. Experience in Clinical Trials and training in Good Clinical Practice are advantages
4. Ability to multi-task, work independently, and manage time effectively
5. Strong communication and interpersonal skills