Director, US Regulatory Affairs - Advertising and Promotion (Hybrid)

Director, Us Regulatory Affairs - Advertising And Promotion (Hybrid)

Location : Cambridge, MA Morristown, NJ

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. As the Director, Us Regulatory Affairs - Advertising And Promotion, you'll partner with other key functional teams to ensure materials are consistent with US regulations, company policy and industry guidelines. You'll be asked to solve problems creatively and strategically, and introduce innovative concepts to more effectively manage ad / promo projects. This is a subject matter expert role with no direct reports, though there will be mentoring, training and team leadership opportunities. We are an innovative global healthcare company with one purpose : to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities :

• Understanding of the U.S. pharmaceutical marketplace and familiarity with medical terminology.
• Understand issues, problems, and opportunities by comparing data from different sources to draw conclusions and then can choose a course of action or develop the appropriate solution.
• Regularly demonstrates the ability to participate in a more strategic capacity in the functional area and day-to-day decision-making process.
• Makes decisions, provides direction and oversight for the day-to-day activities for assigned products, departmental activities, and direct reports.
• In conjunction with the Sr. Director / Product Support Head, imparts senior regulatory guidance and advice during issues management activities; provides oversight and guidance for Rapid Response Teams, and functions as the therapeutic product expert.
• Continually monitors the regulatory environment, interprets new regulations, guidance, and enforcement activities / trends and evaluates the impact on external environments and the business.
• Develops and implements regulatory strategies for marketed products within their product area and mentor and develop others in executing strategy.
• Establishes and develops key internal relationships with therapeutic product leaders to foster open communication and teamwork.
• Assures alignment and consistency in policy application within and across therapeutic products; takes into account the totality of product-related and company activities.
• Assists in ensuring product support relationships with FDA are established and maintained.
• Provides input into the global organization for labeling strategies of marketed drugs.
• Demonstrates significant autonomy in carrying out assigned duties and responsibilities.

About You :

Why Choose Us :

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.