Full Service Regulatory Affairs
ICON’s Global Regulatory Affairs group supports our clients across all divisions to navigate the intricate regulatory agency and ethics committee approval and life cycle challenges.
Global Regulatory Affairs collaborates with our clinical delivery partners to transform complex scientific, medical, and technical data into approvable submission packages using optimised procedures and systems.
We are committed to developing a continuous learning culture – one where we challenge you with engaging work and where your experience adds to your professional development.
Continuous professional development means we are able to progress our peoples’ careers through merit-based promotion.
Our Global Regulatory Affairs leadership team are advocates of mentoring and coaching and have integrated this into our onboarding, functional management and training programmes. With energy, drive and imagination, there’s no limit to where your career can go.
“Within the ICON Regulatory Affairs group there is a Mentor programme for new starters which is coupled with unmatched training and reference materials. My personal growth has involved becoming a Mentor myself where I have enjoyed providing the help to others that I was given at the start of my career.”
Author: Elliot, Senior Regulatory Affairs Associate, UK
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Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader. See all locations Read more