Site Activation Partner

ICON Clinical Research, LP

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

Job Summary

  • ICON plc 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, and contributing to the advancement of innovative treatments and therapies.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

ICON plc 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 document support
  • regulatory requirements input

Nice-to-have

  • fostering inclusive environment
  • driving innovation and excellence
  • advancing innovative treatments
  • diverse and dynamic team
  • well-being and work life balance

Key Requirements

  • Bachelor's degree in life sciences
  • Previous experience in clinical research
  • Previous experience in regulatory affairs
  • Strong attention to detail
  • Organizational skills
  • Excellent communication skills
  • Interpersonal skills
  • Ability to work independently
  • Manage multiple tasks simultaneously

Work Rights

Not specified

Tailored Resume

Cover Letter