Cra I - Chengdu

Syneos Health

Chengdu, China
Fully remote
Conduct on-site and remote monitoring
Review study protocols and informed consent
Ensure gcp guidelines compliance
The role involves conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices

Job Summary

  • The role involves conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
  • Syneos Health is committed to building an inclusive culture where colleagues can authentically be themselves while driving patient progress.
  • Candidates will collaborate with cross-functional teams including investigators and site staff to ensure smooth study conduct.

Matching Summary

The role involves conducting on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.

Skills & Requirements

Must-have

  • Conduct on-site and remote monitoring
  • Review study protocols and informed consent
  • Ensure GCP guidelines compliance
  • Create monitoring plans and checklists
  • Write monitoring reports and action plans

Nice-to-have

  • Passionate problem solvers
  • Collaborative team environment
  • Inclusive culture focus
  • Agile delivery mindset

Key Requirements

  • Bachelor's degree in related field
  • 2-4 years clinical research monitoring experience
  • Strong knowledge of GCP guidelines
  • CCRA certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter