Clinical Trial Associate

ICON

Warsaw, Poland
Clinical trial coordination
Regulatory compliance
Clinical trial documentation management
As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers a range of benefits focused on well-being and work-life balance, including various annual leave entitlements, health insurance options, competitive retirement planning, and a global employee assistance program.
  • ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.

Matching Summary

As a Clinical Trial Associate at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • clinical trial coordination
  • regulatory compliance
  • clinical trial documentation management
  • cross-functional team collaboration
  • clinical trial metrics tracking
  • English proficiency
  • German or French proficiency

Nice-to-have

  • attention to detail
  • excellent organizational skills
  • communication skills
  • fast-paced environment adaptability
  • inclusive work culture

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • B2-level German or French proficiency
  • prior experience or strong interest in clinical research
  • knowledge of clinical trial regulations and guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter