IQVIA
At IQVIA, our Global Regulatory Affairs team partners with pharmaceutical and biotechnology companies worldwide to navigate complex regulatory environments and accelerate access to innovative therapies.
We are seeking an experienced Regulatory Affairs professional with deep expertise in European regulatory affairs and biologic products. This role is ideal for a senior regulatory specialist who enjoys managing complex market applications, lifecycle management activities and post-marketing submissions while acting as a trusted advisor to customers and internal stakeholders.
Joining IQVIA means becoming part of a global team of regulatory experts supporting the development and lifecycle management of medicines that improve patient outcomes around the world.
In this role, you'll have the opportunity to:
If you are passionate about European Regulatory Affairs, biologics and lifecycle management, we'd love to hear from you.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.