Clinical Study Coordinator

5 days ago


Kuala Lumpur, Kuala Lumpur, Malaysia Fortrea Full time

Summary of Responsibilities:

  • Assist in setting up and maintaining tracking systems/spreadsheets for study supplies.
  • Maintain Trial Master File documentation within the appropriate TMF platform, participate in TMF QC, as assigned, and track and archive as applicable.
  • Audit and CAPA tracking.
  • Liaise with vendors, as needed, for study conduct such as printing study materials and/or external systems access for study team members.

Required Skills and Qualifications:

  • Diploma – Associate degree or equivalent.
  • Good oral and written communication skills.
  • Computer literacy (Microsoft Office Suite: Word, Excel, PowerPoint).


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