Editorial summary

The company is seeking a Clinical Trial Project Specialist responsible for overseeing the entire study lifecycle, from planning to closeout, and serving as the primary liaison among sponsors, ethics boards, and monitors. The role involves protocol development, managing study documentation, risk mitigation, safety oversight, and coordinating study logistics, timelines, and vendor engagement. Candidates should possess a degree in Nursing, Science, or Health-related fields. The position offers a salary of up to 6,000 units.

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Job description

[This job id 27002 first appeared in Job-Q.com on 23 Aug 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 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 trial processes.

•        Willing to travel oversea as required for project management

Interested candidates please send in your resume to:

 EA Personnel: Valerie Yong Kian Fung

CEI No.: R1103704

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

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