Ctis Submission Manager

ICON plc

Multiple Locations
Fully remote
Regulatory document preparation
Experience in regulatory affairs
Knowledge of global regulatory requirements
You will play a pivotal role in ensuring regulatory compliance and facilitating the successful execution of clinical trials

Job Summary

  • You will play a pivotal role in ensuring regulatory compliance and facilitating the successful execution of clinical trials.
  • ICON offers a range of additional benefits designed to be competitive within each country.
  • At ICON, inclusion & belonging are fundamental to our culture and values.

Matching Summary

You will play a pivotal role in ensuring regulatory compliance and facilitating the successful execution of clinical trials.

Skills & Requirements

Must-have

  • Regulatory document preparation
  • Experience in regulatory affairs
  • Knowledge of global regulatory requirements

Nice-to-have

  • Excellent communication skills
  • Attention to detail
  • Problem-solving abilities

Key Requirements

  • Bachelor's degree in a scientific field
  • Minimum of 5 years experience
  • Proven ability to manage regulatory submissions

Work Rights

Not specified

Tailored Resume

Cover Letter