Site Activation Partner

ICON

Multiple Locations
Regulatory document preparation
Stakeholder coordination
Record maintenance
ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence

Job Summary

  • ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.
  • As a Study Start Up Associate I, you will play a pivotal role in facilitating the initiation of clinical trials, ensuring compliance with regulatory requirements.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance.

Matching Summary

ICON is a world-leading healthcare intelligence and clinical research organization fostering an inclusive environment driving innovation and excellence.

Skills & Requirements

Must-have

  • regulatory document preparation
  • stakeholder coordination
  • record maintenance
  • study team support
  • study start-up meetings

Nice-to-have

  • foster an inclusive environment
  • drive innovation and excellence
  • advance innovative treatments
  • nurtures talent
  • well-being and work life balance

Key Requirements

  • Bachelor's degree in life sciences
  • Previous experience in clinical research
  • Previous experience in regulatory affairs

Work Rights

Not specified

Tailored Resume

Cover Letter