Number of Applicants
:000+
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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 trial processes.
• 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
RECRUIT EXPRESS PTE LTD
Established since 1996, Recruit Express has emerged as the leading staffing solutions provider that has set a proven track record for matching the right people to the right organization within the shortest time. With our vast network of resources, extensive databases and defined recruitment proce...
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