Senior Informed Consent Specialist

ICON plc

Multiple Locations
Informed consent strategies
Participant-facing materials
Gcp and ethical principles
Lead the development and oversight of informed consent strategies and documents for complex, global clinical studies

Job Summary

  • Lead the development and oversight of informed consent strategies and documents for complex, global clinical studies.
  • Advise study teams on informed consent strategies, including readability, cultural considerations, and local regulatory expectations.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.

Matching Summary

Lead the development and oversight of informed consent strategies and documents for complex, global clinical studies.

Skills & Requirements

Must-have

  • Informed consent strategies
  • Participant-facing materials
  • GCP and ethical principles
  • Global regulatory expectations
  • Stakeholder management skills

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Continuous improvement initiatives
  • Work-life balance opportunities

Key Requirements

  • Bachelor's degree in relevant field
  • Extensive experience in clinical research
  • In-depth knowledge of GCP
  • Exceptional writing and editing skills
  • Proven ability to manage multiple complex studies

Work Rights

Not specified

Tailored Resume

Cover Letter