[University] Clinical Research Coordinator | 5 Months Contract - Toa Payoh

Working Hours: 8:30am - 6pm, Mondays - Fridays

Job Scope:

• Coordinate day-to-day operations of assigned clinical research study.
• Follow up study participants in accordance with IRB-approved protocols.
• Schedule and conduct participant visits (in-person) and follow-ups.
• Collect, enter, and manage study data using REDCAP.
• Maintain regulatory documents and ensure compliance with study protocols, GCP, and institutional guidelines.
• Communicate with participants, research staff, and external collaborators as needed.
• Assist with IRB submissions, amendments, and renewals.
• Prepare for and participate in monitoring visits or audits.
• Assist in study closeout procedures.
• Draw blood from study participants.

Requirements:

• Bachelor’s degree in health sciences, life sciences, psychology, or a related field.
• At least 1–2 years of experience in clinical or academic research settings.
• Solid understanding of GCP, research ethics, and clinical trial operations.
• Experience in regulatory documentation and working with IRBs or REBs.
• Proficiency in EDC platforms (e.g., REDCap), Microsoft Office, and document management systems is a plus.
• Completion of CITI or equivalent human research ethics training preferred.
• Possessing a Certificate in Phlebotomy is preferred.

This hiring is supported by NTUC's e2i.

• Email your resume to [email protected]
• Quote Research Coordinator in the subject line

EA License No: 07C5771