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Responsible for the implementation of complex global regulatory strategies, obtaining and maintaining marketing authorizations for biologic products, and communication of general...
The Director will provide regulatory support across the Therapeutic Areas including Infectious Diseases. Their support includes but is not limited to managing the regulatory...
The Medical Affairs & Patient Partnership Manager provides medical and scientific support, usually focused on a specific franchise and country, externally - to the medical...
Successfully oversee and monitor CRAs in a matrix environment with a focus on quality and timely deliverables; address issues with appropriate team and line manager; direct...
Prepare global regulatory strategies for in vitro diagnostic (IVD) products, direct and prepare regulatory submissions as required for global approvals for in vitro diagnostic...
The GCP/GVP Quality Manager will provide GCP/GVP Auditing and Quality Management support to Santhera’s clinical development program and marketed products to ensure Santhera’s...
Manage and develop the regulatory affairs development team, consisting of global regulatory leads (GRLs) located in Europe and US; Provide guidance and coaching to individual team...
In this exciting role, you will support clinical trial and product license applications for various CMC (Chemistry, Manufacturing and Control) biological projects for customers....
As the Regulatory Affairs Senior Manager, you will manage and support a team of managers and employees of different levels. You will be responsible for developing and implementing...
Implement and execute to a high standard all aspects of assigned clinical studies from designing and planning through to conducting and reporting. Oversee and manage the day-to-day...