Experienced Clinical Research Associate - Full-service- West Coast

Syneos Health

Remote
Remote
Ich-gcp and/or gpp compliance
Site qualification and initiation
Interim monitoring and close-out visits
Perform site qualification, initiation, monitoring, management, and close-out visits ensuring regulatory and protocol compliance

Job Summary

  • Perform site qualification, initiation, monitoring, management, and close-out visits ensuring regulatory and protocol compliance.
  • Maintain working knowledge of ICH/GCP Guidelines, relevant regulations, and company SOPs/processes.
  • Syneos Health offers a supportive culture, career development, and benefits including a company car, health benefits, 401k match, ESPP, and flexible PTO.

Matching Summary

Perform site qualification, initiation, monitoring, management, and close-out visits ensuring regulatory and protocol compliance.

Skills & Requirements

Must-have

  • ICH-GCP and/or GPP compliance
  • Site qualification and initiation
  • Interim monitoring and close-out visits
  • Subject safety and data integrity assessment
  • Investigational product management
  • Investigator Site File (ISF) review

Nice-to-have

  • Adaptability to changing priorities
  • Proactive site suggestion
  • Training junior staff

Key Requirements

  • Bachelor’s degree or RN in a related field
  • Knowledge of Good Clinical Practice/ICH Guidelines
  • Ability to manage required travel of up to 75%

Work Rights

Not specified

Tailored Resume

Cover Letter