Recruit Express will never request for your Singpass details in our recruitment process. Please contact us at 6732 6006 or email to hr.spore@recruitexpress.com.sg if you are unsure if it is a scam.
Recruit Express will never request for your Singpass details in our recruitment process. Please contact us at 6732 6006 or email to hr.spore@recruitexpress.com.sg if you are unsure if it is a scam.
Singapore | Posted: Jul 17, 2026
Responsibilities
• To oversee full study lifecycle from planning to closeout.
• To act as primary liaison between the clinical research sponsors ethics boards, and monitors.
• To lead protocol development to ensure operational feasibility.
• To manage study documents, risk mitigation, safety oversight, and trial master files.
• To coordinate study timelines, vendor engagement, training and logistics
• To Track budgets and provide regular study updates to stakeholders.
• To Coordinate monitoring visits and resolve data queries and quality issues.
Qualification
Degree in Nursing, Science, Health, or Management.
• Minimum 5 years of clinical research experience.
• Strong knowledge of GCP and clinical trial processes.
• Willing to travel oversea as required for project management
Interested candidates please send in your resume to:
recruitment@recruitexpress.com.sg
EA Personnel: Valerie Yong Kian Fung
CEI No.: R1103704
Recruit Express Pte Ltd, EA License No.: 99C4599