Job Summary

• You will conduct remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
• The role requires applying root cause analysis and critical thinking to identify site process failures and implement corrective actions.
• Candidates must ensure audit readiness and maintain collaborative relationships with investigational sites across multiple countries.

Matching Summary

Skills & Requirements

Key Requirements

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

Work Rights