Senior Clinical Research Associate, Sponsor Dedicated

ICON

Clinical trial monitoring
Gcp standards adherence
Phase i oncology experience
You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement

Job Summary

  • You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
  • This is a sponsor‑dedicated role, and our client is seeking a candidate with strong Phase I oncology experience.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance.

Matching Summary

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Skills & Requirements

Must-have

  • Clinical trial monitoring
  • GCP standards adherence
  • Phase I oncology experience
  • Site performance assessment
  • Cross-functional team collaboration

Nice-to-have

  • Independent work and guidance
  • Continuous improvement focus

Key Requirements

  • Bachelor's degree in relevant scientific or healthcare field
  • Extensive experience as a Clinical Research Associate
  • Proven ability to manage multiple sites and projects
  • Expertise in monitoring practices and data integrity
  • Willingness to travel approximately 60%

Work Rights

Not specified

Tailored Resume

Cover Letter