Clinical Trial Assistant (Trial Master File, Clinical Documentation, Sponsor Side) #HDC1

A global life sciences organisation is looking for a Clinical Trial Assistant to support its clinical project teams. You will manage trial documentation and logistics to keep studies compliant and on schedule. What You'll Be Doing • Support clinical project managers and study teams with administration and documentation • Set up, maintain and archive electronic Trial Master Files • File and review study documents for completeness • Support budget tracking and study logistics • Assist with CRO oversight and review processes • Ensure compliance with SOPs, regulations and ICH-GCP • Coordinate study meetings and track actions • Support audit and inspection readiness What You'll Bring • Diploma or Degree in Life Sciences, Pharmacy or a related discipline and above • Experience in clinical trials on the sponsor side is an advantage • Working knowledge of TMF and ICH-GCP is an advantage • Meticulous with strong attention to detail • Strong stakeholder engagement skills • Proficient in Microsoft Office • Able to manage multiple priorities What's In It For You • Exposure to global clinical studies • Structured working environment • Accessible location near MRT Interested? Click Apply or send your updated CV to leonleong@recruitexpress.com.sg Leon Leong De Cong R1551708 Recruit Express Pte Ltd EA License No. 99C4599