Cra I/ii - Shanghai/beijing/guangzhou/wuhan

Syneos Health

Shanghai, China
Fully remote
On-site and remote monitoring
Ensure compliance with gcp
Develop monitoring plans
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices

Job Summary

  • Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
  • Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates.
  • Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct.

Matching Summary

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.

Skills & Requirements

Must-have

  • on-site and remote monitoring
  • ensure compliance with GCP
  • develop monitoring plans
  • collaborate with cross-functional teams
  • accurate and timely documentation

Nice-to-have

  • passionate problem solvers
  • innovating as a team
  • agile and driven to accelerate delivery
  • authentically be yourself
  • diversity of thoughts, backgrounds, cultures, and perspectives

Key Requirements

  • Bachelor's degree or equivalent experience
  • 2-4 years of experience
  • Strong knowledge of GCP
  • CCRA or equivalent certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter