Cra Ii / Senior Cra

ICON

Buenos Aires, Argentina
Fully remote
Conduct site visits
Ensure protocol compliance
Maintain data integrity
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

  • Conduct site visits
  • Ensure protocol compliance
  • Maintain data integrity
  • Collaborate with investigators
  • Resolve data queries

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Contribute to advancement of therapies
  • Nurture talent

Key Requirements

  • Minimum 1.5 years monitoring experience
  • In-depth knowledge of clinical trial processes
  • Knowledge of regulations and ICH-GCP
  • Bachelor's degree scientific/healthcare field

Work Rights

Not specified

Tailored Resume

Cover Letter