Clinical Research Associate, Sponsor Dedicated

ICON plc

Us
Clinical trial monitoring experience
Protocol compliance
Data integrity
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively

Job Summary

  • You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
  • ICON offers a range of additional benefits designed to be competitive and focused on well-being and work-life balance.
  • ICON is committed to providing a workplace free of discrimination and harassment, offering equal consideration for employment.

Matching Summary

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Skills & Requirements

Must-have

  • Clinical trial monitoring experience
  • Protocol compliance
  • Data integrity
  • Patient safety
  • ICH-GCP guidelines

Nice-to-have

  • Fostering an inclusive environment
  • Driving innovation and excellence
  • Collaborative work environment

Key Requirements

  • Minimum 2 years of experience as a Clinical Research Associate
  • Bachelor's degree in scientific or healthcare field
  • Willingness to travel approximately 60%

Work Rights

Not specified

Tailored Resume

Cover Letter