On site
Permanent
[This job id 7213 first appeared in Job-Q.com on 15 May 2026]
Responsibilities
• To oversee full study lifecycle from planning tocloseout.
• To act as primary liaison between the clinicalresearch sponsors ethics boards, and monitors.
• To lead protocol development to ensureoperational feasibility.
• To manage study documents, risk mitigation,safety oversight, and trial master files.
• To coordinate study timelines, vendorengagement, training and logistics
• To Track budgets and provide regular studyupdates to stakeholders.
• To Coordinate monitoring visits and resolve dataqueries and quality issues.
Qualification
· Degree in Nursing, Science, Health, orManagement.
• Minimum 5 years of clinical research experience.
• Strong knowledge of GCP and clinical trialprocesses.
• Willing to travel oversea as required forproject management
Interested candidates please send in your resume to:
valerie@recruitexpress.com.sg
EA Personnel: ValerieYong Kian Fung
CEI No.: R1103704
Recruit Express Pte Ltd, EA License No.: 99C4599
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