Cra Ii / Senior Cra

ICON plc

Buenos Aires, Argentina
Fully remote
Protocol compliance
Data integrity
Patient safety
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

  • 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.
  • 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

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 qualification
  • site initiation
  • site monitoring
  • site close-out visits

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • advancement of innovative treatments
  • work life balance opportunities
  • inclusion & belonging are fundamental

Key Requirements

  • Minimum 1.5 years monitoring experience
  • Bachelor's degree scientific/healthcare
  • In-depth knowledge clinical trial processes
  • ICH-GCP guidelines knowledge
  • Ability to travel at least 60%

Work Rights

Not specified

Tailored Resume

Cover Letter