Research Coordinator

Singapore National Eye Centre; Singapore; On-site; SGD 33,000 - 56,000; Full time

Job summary

National Cancer Centre Singapore Pte Ltd is seeking a Research Coordinator to support oncology trials and related studies. You will assist investigators with patient recruitment, treatment monitoring, data collection, and sample handling where applicable.

The role requires a degree in Health Sciences or a nursing diploma, with at least two years of experience and familiarity with clinical trials. Strong communication and multitasking abilities are essential to succeed in this team.

Qualifications

• Degree in Health Sciences or Diploma in Nursing required.
• 2 years working experience required.
• Experience in Clinical Trials and Good Clinical Practice training is a plus.
• Strong communication and interpersonal skills; ability to multitask.

Responsibilities

• Coordinate ethical/regulatory submissions and renewals.
• Coordinate clinical research studies/trials (screening, recruitment, follow up) and blood/tissue collection if applicable.
• Data collection and management.
• Ensure all research documents are filed properly.
• Assist and prepare for monitoring/audit.

Skills

Multi-tasking

Time management

Communication skills

Interpersonal skills

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: 2 Sept 2026

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 co-ordinating oncology related clinical trials and research studies and assist the Investigators with patient recruitment, monitor of treatment and follow up, collect data and tissue specimens (if applicable) and data management.

Key Responsibilities

• Assist with ethical/ regulatory submissions and renewal
• Coordinate clinical research studies/ trials (Screening, recruitment, follow up) and blood/ tissue specimens collection if applicable
• Data collection and Management
• Ensure all research documents are filed accordingly
• Assist and prepare for monitoring/ audit
• Keep track of research finance budget
• Maintain laboratory supplies and ensure proper collection, handling and shipment delivery if applicable

Job Requirements

• Degree in Health Sciences or Diploma in Nursing
• 2 years working experiences
• Experiences in Clinical Trials and training in Good Clinical Practice are advantages
• Multi-task, independent and good time management,
• Strong communication and interpersonal skills