Cra (level Ii) - Fsp Vaccine - Central Us

Thermo Fisher Scientific UK

Chicago, United States
On-site
Risk-based monitoring approach
Ich-gcp guidelines
Protocol and regulatory compliance
Perform and coordinate all aspects of the clinical monitoring and site management process, including remote or on-site visits to assess protocol and regulatory compliance

Job Summary

  • Perform and coordinate all aspects of the clinical monitoring and site management process, including remote or on-site visits to assess protocol and regulatory compliance.
  • Ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
  • The company offers a comprehensive Total Rewards package including medical, dental, vision plans, employee assistance programs, paid time off, holidays, parental leave, retirement savings, and ESPP.

Matching Summary

Perform and coordinate all aspects of the clinical monitoring and site management process, including remote or on-site visits to assess protocol and regulatory compliance.

Skills & Requirements

Must-have

  • Risk-based monitoring approach
  • ICH-GCP guidelines
  • Protocol and regulatory compliance
  • Investigational product assessment
  • Site processes specialist

Nice-to-have

  • Root cause analysis
  • Critical thinking and problem-solving
  • Collaborative relationships with sites
  • Project publications/tools contribution

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