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.
• Willing to travel oversea as required for project management

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