Clinical Trial Project Specialist HCK

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 5 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

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