Study Start Up Associate, Sponsor Dedicated

ICON

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 inNvative 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 inNvative 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 inNvative treatments and therapies.

Skills & Requirements

Must-have

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

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • advance innovative treatments
  • work life balance opportunities

Key Requirements

  • Bachelor's degree in life sciences
  • Previous experience preferred
  • Strong attention to detail
  • Organizational skills
  • Excellent communication skills
  • Ability to work independently

Work Rights

Not specified

Tailored Resume

Cover Letter