Clinical Trial Project Specialist ( Up 6 K ) #HVN
ExternalS$54K–S$72K/yrFull-timeUnknown1d ago
GCP
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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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Company Intel
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