Cra Ii - Beijing

SyneosHealth

Beijing, China
Fully remote
Conduct on-site and remote monitoring
Review study protocols and informed consent forms
Develop monitoring plans and checklists
Syneos Health is a leading fully-integrated life sciences services organization committed to accelerating customer success in drug development

Job Summary

  • Syneos Health is a leading fully-integrated life sciences services organization committed to accelerating customer success in drug development.
  • The role involves conducting on-site and remote monitoring of clinical research studies to ensure strict compliance with Good Clinical Practice guidelines.
  • Candidates will collaborate with investigators and site staff to resolve issues and ensure smooth clinical trial operations while contributing to process design.

Matching Summary

Syneos Health is a leading fully-integrated life sciences services organization committed to accelerating customer success in drug development.

Skills & Requirements

Must-have

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

Nice-to-have

  • Collaborate with cross-functional teams
  • Participate in SOP development
  • Strong analytical and problem-solving skills
  • Ability to work independently
  • Passionate about patient progress

Key Requirements

  • Bachelor's degree in related field
  • 2-4 years of clinical research monitoring experience
  • Certified Clinical Research Associate (CCRA) preferred

Work Rights

Not specified

Tailored Resume

Cover Letter