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