Clinical Trial Project Specialist #HXW

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:

valerie@recruitexpress.com.sg

EA Personnel: Valerie Yong Kian Fung

CEI No.: R1103704

Recruit Express Pte Ltd, EA License No.: 99C4599