Study Startup Associate Ii

ICON

Regulatory document preparation
Clinical trial compliance
Stakeholder coordination
As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials

Job Summary

  • As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials.
  • You will ensure compliance with regulatory requirements and contribute to the advancement of innovative treatments and therapies.
  • ICON offers a range of additional benefits focused on well-being and work-life balance opportunities for you and your family.

Matching Summary

As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials.

Skills & Requirements

Must-have

  • regulatory document preparation
  • clinical trial compliance
  • stakeholder coordination

Nice-to-have

  • process improvement initiatives
  • cross-functional collaboration
  • inclusive work environment

Key Requirements

  • Bachelor's degree in life sciences
  • minimum of 2 years experience in clinical research
  • strong understanding of regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter