Cra I/ii - Shanghai

Syneos Health

Shanghai, China
Fully remote
On-site and remote monitoring
Ensure compliance with gcp
Develop monitoring plans
Syneos Health is seeking a CRA I/II for their Shanghai location, focusing on clinical research monitoring and compliance with Good Clinical Practice (GCP) guidelines. The role offers opportunities for career development within a supportive culture that values diversity and inclusion

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

Match Score: 85

Syneos Health is seeking a CRA I/II for their Shanghai location, focusing on clinical research monitoring and compliance with Good Clinical Practice (GCP) guidelines. The role offers opportunities for career development within a supportive culture that values diversity and inclusion.

Skills & Requirements

Must-have

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

Nice-to-have

  • passionate problem solvers
  • innovating as a team
  • agile and driven
  • authentically be yourself

Key Requirements

  • Bachelor's degree or equivalent experience
  • 2-4 years of experience in clinical research monitoring
  • Strong knowledge of GCP guidelines
  • Certified Clinical Research Associate (CCRA) preferred

Work Rights

Not specified

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