Sanofi: Global Regulatory Affairs - Specialty Care

Program Goals: 

Gain hands on experience across a variety of specialties within the Global Regulatory Affairs department. Develop a well-rounded understanding of the regulatory functions and drug development process from early stage to post marketing. Lead team meetings, develop regulatory strategy, and contribute to and lead Health Authority submissions with increasing responsibility throughout the Fellowship program. 

Objectives: 

• Develop regulatory strategic skills while contributing to global pre-and post-approval planning and submission. 
• Partner with Medical, Legal, Marketing, and Safety in delivering products for disease globally. 
• Gain experience in the review and approval of promotional materials, including effective feedback skills. 
• Opportunity to engage with global colleagues and learn county/region-specific regulatory processes. 
• Develop strong communication and project management skills.