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The company is seeking a Clinical Trial Project Specialist responsible for overseeing the entire study lifecycle, coordinating study activities, and acting as the primary liaison among sponsors, ethics boards, and monitors. The role requires a degree in Nursing, Science, or Health-related fields, with experience in protocol development, document management, risk mitigation, and safety oversight. The position offers a salary of 9,000, with potential additional compensation up to 6,000. The ideal candidate will possess strong organizational skills and the ability to manage study timelines, budgets, and stakeholder communications.
This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.
[This job id 17632 first appeared in Job-Q.com on 02 Jul 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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Job posting URL: https://singapore.job-q.com/jobs/detail/clinical-trial-project-specialist-up-6-k-hvn-1
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