Study Start Up Associate

ICON plc

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

Job Summary

  • As a Study Start Up Associate I/II/Sr. 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.

Matching Summary

As a Study Start Up Associate I/II/Sr. 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
  • Stakeholder coordination

Nice-to-have

  • Process improvement initiatives
  • Cross-functional team collaboration
  • Inclusive work environment

Key Requirements

  • Bachelor's degree in life sciences
  • Minimum of 1 year experience in clinical research
  • Strong understanding of regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter