Fsp Cra Level 2

Thermo Fisher Scientific UK

Beijing, China
Fully remote
Risk-based monitoring approach
Ich-gcp guidelines compliance
Investigator site initiation
Join a global team supporting top pharmaceutical companies and biotechs in conducting clinical trials across numerous countries

Job Summary

  • Join a global team supporting top pharmaceutical companies and biotechs in conducting clinical trials across numerous countries.
  • Perform and coordinate all aspects of clinical monitoring and site management, ensuring protocol compliance, data reliability, and subject well-being.
  • Conduct remote or on-site visits, assess protocol and regulatory compliance, manage documentation, and ensure audit readiness.

Matching Summary

Join a global team supporting top pharmaceutical companies and biotechs in conducting clinical trials across numerous countries.

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines compliance
  • Investigator site initiation
  • Essential document completion
  • Clinical trial status tracking
  • Root cause analysis

Nice-to-have

  • Customer focus and listening skills
  • Flexibility and adaptability
  • Collaborative team player
  • Problem-solving and critical thinking

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