Fsp Cra (level Ii)

PPD (Thermo Fisher)

Beijing, China
On-site
Risk-based monitoring approach
Ich-gcp guidelines
Site processes specialist
PPD (Thermo Fisher) is seeking a Clinical Research Associate (Level II) for their Beijing office. The role involves monitoring clinical trials, ensuring compliance with protocols and regulations, and managing relationships with investigative sites

Job Summary

  • Perform and coordinate all aspects of the clinical monitoring and site management process, ensuring trial compliance with protocol, regulations, and SOPs.
  • Conduct remote or on-site visits to assess protocol and regulatory compliance, manage documentation, and ensure data reliability.
  • Develop collaborative relationships with investigational sites and ensure audit readiness for subjects' rights, well-being, and data reliability.

Matching Summary

Match Score: 85

PPD (Thermo Fisher) is seeking a Clinical Research Associate (Level II) for their Beijing office. The role involves monitoring clinical trials, ensuring compliance with protocols and regulations, and managing relationships with investigative sites.

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines
  • Site processes specialist
  • Data accuracy through SDR, SDV and CRF review
  • Investigational product assessment
  • Audit readiness
  • Remote or on-site visits

Nice-to-have

  • Collaborative relationships with investigational sites
  • Assist in preparation of project publications/tools
  • Share ideas/suggestions with team members
  • Contribute to process improvement initiatives

Key Requirements

  • Bachelor's degree in life sciences or equivalent
  • 1 year clinical research monitor experience
  • Valid driver's license

Work Rights

Not specified

Tailored Resume

Cover Letter