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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 study updates to stakeholders.
. To Coordinate monitoring visits and resolve data queries and quality issues.
Qualification
Degree in Nursing, Science, Health, or Management.
. Minimum 8 years of clinical research experience.
. Strong knowledge of GCP and clinical trial processes.
Interested candidates please send in your resume to:
[Confidential Information]
EA Personnel: Valerie Yong Kian Fung
CEI No.: R1103704
Recruit Express Pte Ltd, EA License No.: 99C4599
Job ID: 147126515