Site Activation Partner

ICON plc

Multiple Locations
Regulatory document preparation
Ethics committee submissions
Stakeholder coordination
As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies

Job Summary

  • As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.
  • 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.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements, and contributing to the advancement of innovative treatments and therapies.

Skills & Requirements

Must-have

  • regulatory document preparation
  • ethics committee submissions
  • stakeholder coordination
  • record maintenance
  • study document development

Nice-to-have

  • inclusive environment
  • innovation and excellence
  • advancement of treatments
  • diverse and dynamic team

Key Requirements

  • Bachelor's degree in life sciences
  • Previous clinical research experience preferred
  • Previous regulatory affairs experience preferred
  • Ability to work independently
  • Manage multiple tasks simultaneously

Work Rights

Not specified

Tailored Resume

Cover Letter