31 ago - Milano
Parexel
When our values align, there's no limit to what we can achieve.At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will vantaggi a patient. We take our work personally, we do it with empathy and we're committed to making a difference.About the RoleWe are seeking an experienced Regulatory Affairs professional to lead medical devices and combination products regulatory strategy. In this pivotal role, you will provide expert guidance on regulatory pathways for clinical investigations and marketing authorizations, and serve as the key regulatory representative for our global project teams.The role can be home or office based in various European locations.
Key ResponsibilitiesDevelop comprehensive regulatory strategies and technical documentation of medical devices and combination products.Represent the regulatory affairs function in global project teams and governance meetings.Lead regulatory interactions with health authorities and notified bodies, including preparation of documentation and coordination of meetings.Manage regulatory activities throughout the device clinical development lifecycle and marketing authorization.Maintain global regulatory databases with accurate and current information.Collaborate with CMC and QA departments on device change control processes and global submission requirements.Support internal and external audits related to medical device quality systems.Coordinate with cross-functional teams to ensure timely and compliant regulatory submissions.Contribute to continuous improvement initiatives, innovation, and strategic planning within the regulatory function.Skills and Experience:University degree in a scientific discipline, technical or
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