Clinical Research Associate Ii (cra Ii) – Fsp Business Unit

Thermo Fisher Scientific UK

UK
Fully remote
Bachelor's degree in life sciences
Valid driver's license
Risk-based monitoring approach
The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials

Job Summary

  • The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
  • Candidates will apply root cause analysis and critical thinking to identify site process failures and implement corrective actions to ensure data reliability.
  • The position requires frequent travel of 60-80% to investigate sites, participate in investigator meetings, and maintain audit readiness across global locations.

Matching Summary

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

Skills & Requirements

Must-have

  • Bachelor's degree in life sciences
  • Valid driver's license
  • Risk-based monitoring approach
  • ICH-GCP guidelines knowledge
  • Critical thinking and problem solving

Nice-to-have

  • Collaborative relationship building
  • Process improvement initiatives
  • Flexible and adaptable mindset
  • Strong presentation skills
  • Effective oral communication

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter