Clinical Trial Coordinator

2 weeks ago


Hong Kong, Central and Western District, Hong Kong SAR China HON Fortrea Hong Kong Limited Full time

Job Summary:

The Clinical Trial Administrator will be responsible for the execution of a Clinical Research Project. This role will involve communicating with project team members, maintaining documentation, and ensuring timely production of high-quality clinical data.

Key Responsibilities:

  • Document and track study activities using relevant forms and tools
  • Assist in the preparation of study and site-specific materials
  • Complete minute-taking and documentation for sponsor/external or internal teleconferences
  • Provide support for Investigator Meetings and track meeting attendees
  • Maintain Trial Master File documentation and participate in TMF QC
  • Audit and CAPA tracking
  • Set up and maintain clinical investigator files and documentation
  • Liaise with vendors for study conduct
  • Coordinate and plan study supply shipments
  • Generate reports as needed

Requirements:

  • Minimum one year administrative experience or equivalent training
  • Good oral and written communication skills
  • Good organizational and time management skills
  • Computer literacy (Microsoft Office Suite)

About Fortrea:

Fortrea is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions.



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