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
Nice-to-have
foster an inclusive environment
drive innovation and excellence
continuous improvement initiatives
Key Requirements
Bachelor's degree in relevant scientific discipline