Clinical Site Associate

ICON Broadbean

United States Of America
Experience as a study coordinator
Site compliance management
Document management skills
ICON plc is a world-leading healthcare intelligence and clinical research organization

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization.
  • In this role, you will play a pivotal part in supporting clinical trial operations.
  • ICON offers a range of additional benefits focused on well-being and work-life balance.

Matching Summary

ICON plc is a world-leading healthcare intelligence and clinical research organization.

Skills & Requirements

Must-have

  • Experience as a Study Coordinator
  • Site compliance management
  • Document management skills

Nice-to-have

  • Strong organizational skills
  • Ability to work collaboratively
  • Attention to detail

Key Requirements

  • Bachelor’s degree in Life Sciences or Healthcare
  • Minimum of one year of clinical research experience

Work Rights

Not specified

Tailored Resume

Cover Letter