Remote IVD Regulatory Affairs Lead – EU IVDR Expert

Parexel International is seeking an experienced Regulatory Affairs professional to lead IVD regulatory strategy, provide expert guidance on performance evaluation studies, and oversee regulatory paths for marketing authorisations with global project teams.The role supports EU IVDR, ISO 13485 knowledge and interacts with health authorities; flexible location...

Overview In this Regulatory Affairs Lead role, you shape IVD regulatory strategies, guiding performance evaluation and marketing authorizations. You will act as the regulatory lead for global project teams, coordinating interactions with authorities and ensuring compliant submissions. The role supports lifecycle management and continuous improvement within...

Parexel International is seeking an experienced Regulatory Affairs professional to lead IVD regulatory strategy, provide expert guidance on performance evaluation studies, and oversee regulatory paths for marketing authorisations with global project teams. The role supports EU IVDR, ISO 13485 knowledge and interacts with health authorities; flexible location...

Parexel International is seeking an experienced Regulatory Affairs professional to lead IVD regulatory strategy, provide expert guidance on performance evaluation studies, and oversee regulatory paths for marketing authorisations with global project teams. The role supports EU IVDR, ISO 13485 knowledge and interacts with health authorities; flexible location...

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...

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...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global...

Parexel is seeking an experienced Regulatory Affairs professional to lead IVD regulatory strategy across European projects.È il candidato/la candidata ideale per questa opportunità? Lo scopra leggendo la panoramica del ruolo qui sotto.You will guide regulatory pathways for performance evaluation studies and marketing authorizations, serving as the

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 International is seeking an experienced Regulatory Affairs professional to lead IVD regulatory strategy, provide expert guidance on performance evaluation studies, and oversee regulatory paths for marketing authorisations with global project teams. The role supports EU IVDR, ISO 13485 knowledge and interacts with health authorities; flexible location...

Parexel International is seeking an experienced Regulatory Affairs professional to lead IVD regulatory strategy, provide expert guidance on performance evaluation studies, and oversee regulatory paths for marketing authorisations with global project teams.The role supports EU IVDR, ISO 13485 knowledge and interacts with health authorities; flexible location...

Parexel International is seeking an experienced Regulatory Affairs professional to lead IVD regulatory strategy, provide expert guidance on performance evaluation studies, and oversee regulatory paths for marketing authorisations with global project teams.The role supports EU IVDR, ISO 13485 knowledge and interacts with health authorities; flexible location...

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...