Clinical Research Associate

Full Time
2 years ago

Job description

  • Primarily responsible for coordinating the various aspects of clinical trials. Works as part of a clinical delivery team providing support, guidance and advice on a local level. Develops existing tools and processes to identify areas of improvement and ensures business continuity for study delivery. Able to solve complex problems within a range of studies.
  • Be responsible for initiating, organising and managing the assigned studies.
  • On site monitoring and site managements for global studies.
  • Ensure clinical trials conducted in compliance with protocol & GCP.
  • Ensure clinical trials can be conducted per timeline requirement.


  • University education in pharmacy related field
  • Good command in English
  • Ability to manage multiple priorities and work effectively within cross-functional team
  • Excellent interpersonal and communication skill
  • Detail-orientated, self-starter, and organized person


  • Bachelor degree or above, major in pharmacy or health science related background.
  • At least 2 year experience in the role of CRA including on-site monitoring.
  • With knowledge in GCP clinical therapeutics, study methodology, GCP.
  • Excellent command of English (both written and spoken).
  • Good interpersonal skills, a good team player, and computer skills.
  • Be able to prioritize and manage multiple tasks.

Job contact: will be available on November 8, 2021.