Clinical Trials Coordinator

Ng Teng Fong General Hospital; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

Ng Teng Fong General Hospital is seeking a qualified Clinical Research Coordinator to support principal investigators in overseeing study conduct, ensure ethical and regulatory compliance, and assist with data collection and documentation.

The role requires a Bachelor's Degree in Nursing or Health Sciences, strong communication, and the ability to manage multiple projects in a fast-paced setting; experience with phlebotomy and MS Office is preferred.

Qualifications

• Bachelor's Degree in Nursing/Health Sciences or relevant field.
• Ability to perform phlebotomy preferred.
• Hands on experience with inpatient and/or clinic work processes preferred.
• Proficiency in MS office applications.
• Excellent verbal and written communication skills.
• Good interpersonal and communication skills.
• Ability to speak local languages is preferred.
• Strong initiative and drive in a fast-paced setting.

Responsibilities

• Support principal investigators by facilitating study matters and ensuring proper conduct and implementation of research activities.
• Manage multiple projects including data collection and simple statistic calculations; report and file data sheets regularly.
• Ensure accurate and audit-ready source documentation and logs.
• Maintain completed project files and uphold patient confidentiality.
• Coordinate with internal/external agencies, investigators and teams to ensure project success.
• Assist in recruitment/consenting/interim & final analyses/audits as needed.
• Monitor clinical projects to ensure timelines and deliverables are met.
• Perform other duties as directed by supervisors, PI and HOD.

Skills

Phlebotomy

MS Office

Verbal and written communication

Interpersonal skills

Initiative

Fast-paced environment

Education

Bachelor's Degree in Nursing/Health Sciences

Tools

MS Office

Job description

Ng Teng Fong General Hospital is seeking a qualified Clinical Research Coordinator to support principal investigators in overseeing study conduct, ensure ethical and regulatory compliance, and assist with data collection and documentation.

The role requires a Bachelor's Degree in Nursing or Health Sciences, strong communication, and the ability to manage multiple projects in a fast-paced setting; experience with phlebotomy and MS Office is preferred.