Senior Informed Consent Specialist

ICON Clinical Research, LP

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

Job Summary

  • You will lead the development and oversight of informed consent strategies and documents for complex, global clinical studies.
  • Key responsibilities include leading the creation, review, and optimisation of global and country-specific informed consent forms for complex or high-risk studies.
  • 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

You will 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
  • manage complex studies

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