Clinical Research Associate Ii

ICON Clinical Research, LP

Portugal
Protocol compliance
Data integrity
Patient safety
As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials, ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • In addition to your competitive salary, 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 II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • protocol compliance
  • data integrity
  • patient safety
  • site monitoring visits
  • ICH-GCP guidelines

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • advancement of innovative treatments
  • work life balance opportunities

Key Requirements

  • Minimum of 2 years of experience as a Clinical Research Associate
  • Bachelor's degree in a scientific or healthcare-related field
  • Fluent English
  • Ability to travel at least 60% of the time
  • Possess a valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter