Research Coordinator: Drive Studies & Data Integrity

NATIONAL UNIVERSITY HEALTH SERVICES GROUP PTE. LTD.; Singapore; On-site; SGD 42,000 - 64,000; Full time

Job summary

National University Health Services Group Pte. Ltd. is seeking a Clinical Research Coordinator to support the Principal Investigator and the Family Medicine Development team in delivering timely research outcomes.

The role covers project management, recruitment, data collection, entry, and analysis, with liaison to partnering institutions as needed. You will manage study timelines, regulatory documents, and audits, while maintaining accurate study files and administrative support across sites.

Qualifications

• Bachelor’s degree in health sciences or nursing.
• Strong interpersonal and communication skills, both written and verbal.
• Ability to work independently and as part of a team.
• Proficient in MS Office applications (Word, Excel, PowerPoint).
• Meticulous, organized and detail-oriented.

Responsibilities

• Coordinate all aspects of a research project from start-up to close-out.
• Prepare, maintain regulatory documents and study files.
• Manage study timelines and budgets, track resources.
• Screen and recruit potential study participants and obtain informed consent.
• Collect, enter, and manage study data; ensure data quality and integrity.
• Ensure adherence to IRB guidelines and regulatory requirements; assist audits.
• Provide administrative support to the PI and study team; organize meetings.

Skills

Interpersonal skills

Verbal & written communication

Organizational skills

Time management

MS Office proficiency

Attention to detail

Education

Bachelor’s degree in health sciences or nursing

Tools

MS Office Suite

Electronic data capture systems

Job description

National University Health Services Group Pte. Ltd. is seeking a Clinical Research Coordinator to support the Principal Investigator and the Family Medicine Development team in delivering timely research outcomes.

The role covers project management, recruitment, data collection, entry, and analysis, with liaison to partnering institutions as needed. You will manage study timelines, regulatory documents, and audits, while maintaining accurate study files and administrative support across sites.