Clinical Trial Assistant

ICON Clinical Research, LP

Paris, France
Coordination and administration of clinical trials
Maintain and organize clinical trial documentation
Support preparation of study materials
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

  • Coordination and administration of clinical trials
  • Maintain and organize clinical trial documentation
  • Support preparation of study materials
  • Track and report clinical trial metrics

Nice-to-have

  • Foster an inclusive environment
  • Contribute to advancement of therapies
  • Work collaboratively in fast-paced environment

Key Requirements

  • Bachelor's degree in scientific or healthcare field
  • Prior experience or strong interest in clinical research
  • Knowledge of clinical trial processes
  • Excellent organizational and communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter