Clinical Trial Assistant

ICON Broadbean

Paris, France
Clinical trial documentation management
Study-related material preparation
Cross-functional team collaboration
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

  • Clinical trial documentation management
  • Study-related material preparation
  • Cross-functional team collaboration
  • Clinical trial metrics tracking
  • Regulatory requirements compliance

Nice-to-have

  • Fostering inclusive environment
  • Driving innovation and excellence
  • Advancing innovative treatments
  • Work-life balance opportunities

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Prior experience in clinical research
  • Knowledge of clinical trial processes
  • Ability to work collaboratively
  • Attention to detail

Work Rights

Not specified

Tailored Resume

Cover Letter