Cra/scra

ICON plc

Not specified
Conduct site visits
Ensure protocol compliance
Data review and query resolution
ICON plc is seeking a Clinical Research Associate II to contribute to clinical trial design and execution, ensuring compliance and data integrity. The role requires a Bachelor's degree and a minimum of two years of relevant experience, alongside strong organizational and communication skills

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

Match Score: 85

ICON plc is seeking a Clinical Research Associate II to contribute to clinical trial design and execution, ensuring compliance and data integrity. The role requires a Bachelor's degree and a minimum of two years of relevant experience, alongside strong organizational and communication skills.

Skills & Requirements

Must-have

  • Conduct site visits
  • Ensure protocol compliance
  • Data review and query resolution
  • Prepare study documentation
  • ICH-GCP guidelines knowledge

Nice-to-have

  • Foster inclusive environment
  • Drive innovation and excellence
  • Contribute to advancement of therapies
  • Work life balance opportunities

Key Requirements

  • Minimum 2 years CRA experience
  • Bachelor's degree scientific/healthcare
  • Travel at least 60% of the time
  • Valid driver’s license

Work Rights

Not specified

Tailored Resume

Cover Letter