Clinical Research Associate

AstraZeneca

On-site monitoring experience
Global study management
Protocol and gcp compliance
The role is primarily responsible for coordinating various aspects of clinical trials as part of a clinical delivery team

Job Summary

  • The role is primarily responsible for coordinating various aspects of clinical trials as part of a clinical delivery team.
  • Candidates must ensure clinical trials are conducted in strict compliance with the protocol and Good Clinical Practice (GCP).
  • AstraZeneca embraces diversity and equality of opportunity, committed to building an inclusive and diverse team representing all backgrounds.

Matching Summary

The role is primarily responsible for coordinating various aspects of clinical trials as part of a clinical delivery team.

Skills & Requirements

Must-have

  • On-site monitoring experience
  • Global study management
  • Protocol and GCP compliance

Nice-to-have

  • Excellent English communication skills
  • Strong interpersonal team player
  • Ability to prioritize multiple tasks

Key Requirements

  • Bachelor degree or above
  • At least 2 years CRA experience
  • Major in pharmacy or health science
  • Knowledge in GCP clinical therapeutics

Work Rights

Not specified

Tailored Resume

Cover Letter