Editorial summary

The company is seeking a Clinical Trial Project Specialist responsible for managing the full study lifecycle, including protocol development, documentation, risk mitigation, and safety oversight. The role involves coordinating study timelines, vendor engagement, training, and logistics, as well as tracking budgets and ensuring quality through monitoring visits. Candidates should possess a degree in Nursing, Science, or Health-related fields. The position offers a salary of up to 6,000 units.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job id 28844 first appeared in Job-Q.com on 31 Aug 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:

 EA Personnel: ValerieYong Kian Fung

CEI No.: R1103704

Recruit Express Pte Ltd, EA License No.: 99C4599

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