Clinical Research Associate

ICON

Slovakia
Clinical trial site monitoring
Good clinical practice (gcp) standards
Clinical trial data collection and reporting
As a Clinical Research Associate 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 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.
  • ICON offers a diverse culture that rewards high performance and nurtures talent, with competitive salary and a range of benefits focused on well-being and work-life balance.
  • ICON is committed to providing an inclusive and accessible environment for all candidates and a workplace free of discrimination and harassment.

Matching Summary

As a Clinical Research Associate 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

  • Clinical trial site monitoring
  • Good Clinical Practice (GCP) standards
  • Clinical trial data collection and reporting
  • Site performance assessment
  • Clinical trial software proficiency
  • Travel at least 60% of the time

Nice-to-have

  • Strong organizational skills
  • Problem-solving skills
  • Effective stakeholder management
  • Training and guidance provision
  • Inclusive and diverse culture

Key Requirements

  • Advanced degree in life sciences, nursing, or medicine
  • 3-6 years experience as Clinical Research Associate
  • Valid driver’s license
  • Ability to travel at least 60%

Work Rights

Not specified

Tailored Resume

Cover Letter