Manager Regulatory Affairs Advertising and Promotion

Sanofi; New Jersey; Hybrid; USD 110,000 - 150,000; Full time

Job summary

Sanofi is seeking a Manager Regulatory Affairs Advertising and Promotion to join our Cambridge, MA / Morristown, NJ team. You will drive regulatory strategies for advertising and promotion, partner with brand teams, and ensure compliant US submissions across products.

The role requires 1+ year in regulatory affairs with experience in advertising and promotion, strong cross-functional collaboration, and the ability to navigate complex scientific topics with ethical judgment in a dynamic biotech

Qualifications

• Bachelor’s degree from an accredited four-year college or university; Science focus preferred, but not required.
• Experience in pharmaceutical or medical device Regulatory Affairs (1–3 years).
• Experience with Advertising and Promotion in Regulatory required.

Responsibilities

• Identifies product-specific or therapeutic area A&P issues and proposes solutions.
• Advises on risk/benefit of regulatory actions and supports business decisions.
• Oversees regulatory strategic objectives and projects with minimal supervision.
• Acts as Regulatory representative on brand teams and Review Committees for commercial and medical materials.
• Provides input on domestic regulatory strategies and lifecycle management programs.
• Contributes regulatory expertise to labeling on new and supplemental applications.

Skills

Regulatory affairs

Advertising & promotion

Cross-functional collaboration

Oral communication

Written communication

US pharmaceutical market

Ethics & integrity

Education

Bachelor’s degree in science

Job description

Manager Regulatory Affairs Advertising and Promotion# Sanofi Careers## Manager Regulatory Affairs Advertising and PromotionBewerben: Cambridge, MA: Morristown, NJ: Vollzeit: Gestern ausgeschrieben: Enddatum: 29. Oktober 2026 (Noch 6 Tage Zeit für Bewerbung): R2875782**Job title:** Manager Regulatory Affairs Advertising and Promotion* **Location:** Cambridge, MA / Morristown, NJ **About the job** Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. **About Sanofi** We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.**Main Responsibilities:*** Identifies product-specific or therapeutic area A&P issues and works with other teams to propose and implement solutions.* Identifies different strategies for addressing issues; advises of risk/benefit of each and assists clients with making sound business decisions with the understanding of the potential risk/benefits with respect to intervening regulatory matters.* Oversees and bears responsibility for the successful implementation of regulatory strategic objectives and projects with minimal supervision.* Active participant and Regulatory representative on brand teams and Review Committees (RC) for commercial and medical materials, respectively.* Provides guidance and feedback to internal Sanofi constituencies (commercial groups, R&D) to maximize the competitive impact of product development as well as ultimate promotion, advertising, and reimbursement. Provides input to the Global organization on domestic regulatory strategies for in-line products through life cycle management programs.* Contribute A&P expertise to the development of optimal labeling on new and supplemental new drug applications.* Provides product-specific Regulatory strategies to mitigate risk; works in conjunction with brand team management to provide advice and risk/benefit analysis to maximize value to stakeholders.* Performs other duties as assigned. **About You** Basic Qualifications:* Bachelor’s degree from an accredited four-year college or university; Science focus preferred, but not requireWork Experience Required:* 1+ Years experience in the following areas: + Experience within pharmaceutical or medical device Regulatory Affairs. + Successful track record with ideally 1-3 years relevant regulatory experience. + Dealt effectively with cross-functional groups, which may include Medical, Legal, Marketing etc.* Experience in Advertising and Promotion in Regulatory required.* Dealt effectively with cross-functional groups, which may include Medical, Legal, Marketing etc.Knowledge, Skills and Equivalent Experience:* Knowledge and understanding of complex medical and scientific subject matter.* Ability to work well within cross-functional teams.* Demonstrates solid oral communication and writing skills.* Understanding of the U.S. pharmaceutical marketplace, and familiarity with medical terminology.* 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.* Develops and proposes 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 to gain acceptance of ideas or plans.* Can build collaborative internal networks to obtain cooperation.* Unquestionable ethics, professional integrity and personal values consistent with the Sanofi values.* Is able to balance 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 manage workload. Is able to multi-task 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.* Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.* Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.* Help improve the lives of millions of people globally by making drug development quicker and more effective. Sanofi Inc. and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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. #GD-SA #LI-SA#LI-Hybrid