Editorial summary

The company is seeking a Clinical Trial Project Specialist to oversee the full study lifecycle from planning to closeout, serving as the primary liaison among sponsors, ethics boards, and monitors. The role involves leading protocol development, managing study documents and risk mitigation, coordinating timelines, vendor engagement, training, and logistics, and tracking budgets with regular updates to stakeholders. Key requirements include a degree in nursing, science, or health-related fields, along with experience in safety oversight, trial master file management, and data quality issue resolution. Compensation is up to 6,000 currency units.

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

Job description

[This job https://singapore.job-q.com/jobs/detail/clinical-trial-project-specialist-up-6-k-hvn-40537 first appeared in Job-Q.com on 29 Oct 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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