You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively
Job Summary
You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.
Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
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 contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.
Skills & Requirements
Must-have
site start-up and activation
regulatory document preparation
clinical trial applications
ethics committee submissions
stakeholder coordination
ICH-GCP compliance
Nice-to-have
process improvement initiatives
fostering an inclusive environment
driving innovation and excellence
advancement of innovative treatments
Key Requirements
Bachelor's degree in life sciences
Minimum of 2 years experience
Clinical research or regulatory affairs experience