Senior Site Specialist

ICON Broadbean

Multiple Locations
Regulatory document preparation
Clinical trial applications
Study start-up activities
As a Senior Study Start Up Associate at ICON, you will play a pivotal role in leading the initiation of clinical trials

Job Summary

  • As a Senior Study Start Up Associate 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.
  • ICON offers a range of benefits designed to support well-being and work-life balance for you and your family.

Matching Summary

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

Skills & Requirements

Must-have

  • Regulatory document preparation
  • Clinical trial applications
  • Study start-up activities

Nice-to-have

  • Process improvement initiatives
  • Collaboration with cross-functional teams
  • Inclusive work environment

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum of 4 years of experience
  • Strong understanding of regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter