Our client is seeking a dedicated and detail-oriented Research Coordinator (1 year contract) to support the planning, execution, and coordination of research programmes and projects.
This role offers the opportunity to work closely with investigators, stakeholders, and research participants to ensure projects are delivered successfully, ethically, and in compliance with regulations.
Key Responsibilities
- Plan, coordinate, and monitor assigned research programmes and projects.
- Manage project funding, expenditure, purchases, and funder correspondence.
- Support grant processes, including claims, verification, and variation submissions.
- Facilitate progress tracking, review meetings, and timely reporting.
- Prepare reports, presentations, and study-related documentation.
- Provide research administration support (IRB submissions, research agreements, etc.).
- Assist with participant recruitment, consent-taking, and queries.
- Maintain accurate study records and manage research data (extraction, cleaning, compliance).
- Contribute to organisational projects and events as required.
Requirements
- Bachelor's degree in Science, Public Health, or Social Science (Entry-levels are welcome)
- Knowledge of Good Clinical Practice (GCP) guidelines and the Human Biomedical Research Act (HBRA) is an advantage.
- Strong interpersonal and communication skills; able to work independently and in teams.
- Meticulous, well-organised, and capable of multi-tasking in a fast-paced environment.
- Demonstrates accountability, leadership, and adaptability to meet research deliverables.
- Willingness to travel between hospitals and external study sites.
Work Hours
- Monday to Friday: 8:00 AM – 4:30 PM
- Saturday: 8:00 AM – 12:30 PM
How to Apply:
If interested, please send your resume to or by clicking the Apply Now button.
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