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.: R