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