Clinical Research Associate

4 days ago


Hong Kong, Central and Western District, Hong Kong SAR China ICON Full time

At ICON, we are dedicated to making a positive impact on people's lives. We do this by working alongside our clients to deliver innovative solutions that help them develop life-changing medicines.

This role is an exciting opportunity for you to be part of a global team that plays a key role in the success of clinical trials at a local level.

  • Provide administrative support to other members of the clinical study team, ensuring the smooth tracking of study progress.
  • Collaborate with site staff to ensure clinical trials are conducted according to protocol.
  • Manage documentation, track, and review electronic files.
  • Be responsible for IRB/EC and RA submissions from initial submission to amendment.
  • Support the study start-up process locally.

You will have the opportunity to experience the full lifecycle of a project and genuinely contribute to drug development and improving patients' lives.

Key Requirements:
  • Detail-oriented, passionate, and reliable.
  • A relevant educational background in life sciences or as a licensed healthcare professional.
  • Strong interpersonal skills.
  • Proficiency in MS Office.
  • The ability to manage multiple priorities simultaneously.
  • A quality-focused mindset.
  • Oncology trial experience is a plus.


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