Regulatory Affairs Consultant: Medical Device and Combination Product Expert

Job description

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 benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. About the Role: We 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 Responsibilities: Develop comprehensive regulatory strategies and technical documentation of medical devices and combination products. Represent the regulatory affairs function in global project teams and governance meetin...