Job Title: Senior Director, Global Advertising and Promotion Therapeutic Area Head

Location: Bridgewater, NJ / Cambridge, MA (must adhere to hybrid working schedule of being onsite 3x per week)

About the Job

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.

In this role, you will be responsible for the oversight of regulatory review of advertising, promotion, medical, media relations and other internal and external communications related to company products in one or more therapeutic areas. You will play an important role in mentoring and developing direct reports for future leadership roles. You will also provide input into the global organization for promotional strategies, including launch strategies. Additionally, you will be the primary therapeutic area liaison with FDA’s Office of Prescription Drug Promotion (OPDP) for drugs, Advertising & Promotional Labeling Branch (APLB) for biologics, and Division of Premarket and Labeling Compliance (DPLC) for medical devices, as applicable.

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

In conjunction with the Global Regulatory Affairs' Head of Global Advertising & Promotion, recommend and contribute to the development of strategic objectives across assigned therapeutic areas.

Contribute to the maintenance and enhancement of strategic relationships with customers.

Ensure that the regulatory environment is continually monitored for new regulations/guidance and applicable enforcement activities.

Oversee staff implementation of U.S. Regulatory strategies (e.g., submissions, product defense, labeling development, FDA enforcement, clinical trial support, FDA contacts).

Provide opportunities for direct reports that contribute to Global Advertising & Promotion staff development.

Contribute to the maintenance and enhancement of strategic relationships with customers and direct activities to influence the external regulatory environment in accordance with GRA priorities. 

Establish and develop key internal relationships with R&D and Regulatory Development to foster open communication and teamwork.

Ensure alignment and consistency in Global Advertising & Promotion policy application within and across therapeutic products; taking into account the totality of product-related and company activities.

Ensure therapeutic product relationships with FDA are established and maintained.

Performs other duties as assigned.

About You

Experience

Successful track record in Regulatory Affairs with 7 -10+ years of relevant experience in Regulatory Advertising & Promotion within the pharmaceutical or medical device industry.

Experience managing others is required.

Possess a depth of experience dealing effectively with cross-functional groups, which may include Medical, Legal, Marketing, etc.

Education

Bachelor’s degree from an accredited four-year college or university in a Life Sciences discipline or related scientific field.

Advanced degree is highly preferred.

Technical Skills

Extensive knowledge and understanding of complex medical and scientific subject matter.

Possesses comprehensive breadth of technical knowledge in regulatory affairs and ensures dissemination of this knowledge to others throughout the organization.

Ability to work well within cross-functional teams.

Can demonstrate solid oral communication and writing skills.

Understanding of the U.S. pharmaceutical market place, and familiarity with medical terminology.

Understanding of Global Advertising & Promotion requirements preferred.

Understands 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.

Develops collaborative relationships to facilitate the accomplishment of work goals.

Generates innovative solutions in work situations, trying different and novel ways to deal with work problems and opportunities.

Shows ability to use appropriate interpersonal styles and techniques and can modify behavior to gain acceptance of ideas or plans.

Can build networks to obtain cooperation without relying on authority.

Unquestionable ethics, professional integrity and personal values consistent with Sanofi values.

Capable of managing therapeutic product projects on topics specific to the functional area.  Is able to balance managing these projects with day-to-day duties, ensuring participation from other members of the department as needed.

Is able to establish priorities and timelines to effectively self-manage workload. Is able to multi-task exceptionally well.

Deals with people in an honest and forthright manner representing information and data accurately. 

Why Choose Us?

Bring the miracles of science to life alongside a supportive, future-focused team.

Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

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.

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Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.