Cta

ICON plc

Warsaw, Poland
Hybrid
Assist with design and analysis
Interpret medical data
Coordinate clinical trials
As a Clinical Trial Administrator 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 Administrator 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.
  • Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
  • 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

As a Clinical Trial Administrator 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

  • assist with design and analysis
  • interpret medical data
  • coordinate clinical trials
  • maintain trial documentation
  • support study material preparation
  • track and report metrics

Nice-to-have

  • foster inclusive environment
  • drive innovation and excellence
  • shape future of clinical development
  • work collaboratively
  • attention to detail

Key Requirements

  • Bachelor's degree scientific/healthcare
  • Prior experience clinical research
  • Knowledge clinical trial processes
  • Excellent organizational skills
  • Excellent communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter