Clinical Research Associate

le contenu du travail

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.

職務說明

• Be responsible for initiating, organizing 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.
  
  

資歷

• 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.