Cra Ii

Thermo Fisher Scientific UK

Fully remote
Bachelor's degree in life sciences
Valid driver's license required
60-80% travel frequency
The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for clinical trials

Job Summary

  • The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for clinical trials.
  • Candidates will apply root cause analysis and problem-solving skills to identify site process failures and implement corrective actions.
  • This position requires frequent travel of 60-80% to investigate sites and ensure adherence to ICH-GCP guidelines and applicable regulations.

Matching Summary

The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing documentation for clinical trials.

Skills & Requirements

Must-have

  • Bachelor's degree in life sciences
  • Valid driver's license required
  • 60-80% travel frequency
  • ICH-GCP guidelines knowledge
  • Risk-based monitoring approach
  • Root cause analysis skills

Nice-to-have

  • Strong critical thinking abilities
  • Effective oral communication skills
  • Collaborative team relationship building
  • Flexible adaptability to scenarios
  • Process improvement contributions

Key Requirements

  • 1 year experience as clinical research monitor
  • Bachelor's degree in life sciences
  • Registered Nursing certification or equivalent
  • Completion of PPD Drug Development Fellowship
  • Valid driver's license where applicable

Work Rights

Not specified

Tailored Resume

Cover Letter