Clinical Trial Assistant

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  Responsibilities:

  • Understand GCP and SOP of clinical research
  • Assist CRM/PM/ CRA to prepare and maintain study document
  • Review in-house documents, track and review Investigational Product and other materials
  • Assist to resolve all outstanding DCFs as applicable
  • Assist site payment and tracking
  • Actively implement quality control procedures. Maintain high quality standards, through accuracy and quality of work
  • Generate regular assigned reports and prepare presentation slides
  • Responsible for filing and archiving of clinical documents

Qualifications:

  • College degree. Pharmacology or biology preferred.
  • Good communication, coordination and organization skills
  • Good analytical and problem solving skill
  • Prefer to have good command of English in speaking, listening, reading and writing
  • Familiar with IT software e.g. Microsoft Word, Excel,