Clinical Research Associate Ii Or Senior

ICON Clinical Research, LP

Sao Paulo, Brazil
Clinical trial monitoring activities
Protocol compliance
Data integrity
As a Clinical Research Associate at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Research Associate at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
  • 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 within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Clinical Research Associate at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

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

Nice-to-have

  • Inclusive environment
  • Foster innovation and excellence
  • Work life balance opportunities

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Solid experience as a Clinical Research Associate
  • In-depth knowledge of clinical trial processes
  • Willingness to travel approximately 60%

Work Rights

Not specified

Tailored Resume

Cover Letter