Job title: Global Regulatory StrategistLocation: Morristown, NJ/ Cambridge, MAAbout the jobOur team is involved in developing regulatory product strategies for the oncology therapeutic area, leading regulatory efforts in the development stage of drug products. 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?The Regulatory Strategist provides regulatory expertise and guidance on procedural and documentation requirements to GRT and cross-functional teams working flexibly within and across regions to ensure delivery of business objectives.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 SanofiWe'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 responsibilitiesCross - Functional CollaborationEnables the Global Regulatory Lead (GRL) by providing quality regulatory input and positioning to internal business partners, including clinical development teams, commercial teams, and the Global Regulatory Team (GRT) for assigned projectsLiaises with nonclinical, clinical, CMC, commercial, and other internal business partners in partnership with the GRL to enable successful regulatory outcomesContributes to a harmonized, One Sanofi regulatory voice through participation in appropriate committees and forums, at the direction of the GRLProactively contributes to the GRT with curiosity and openness to diverse perspectives, providing strategic input on the Target Product Profile (TPP), business planning, governance, and committees; may be requested to lead GRT meetingsHealth Authority (HA) EngagementAccountable for developing HA engagement and interaction plans for assigned products, including: (1) authoring briefing documents focused on strategy and scientific content and leading team meeting preparationsMay lead HA meetings and preparations as designatedMay serve as regional/local regulatory lead and point of contact with Health Authorities for projects/products within remit, as neededRegulatory Submissions & OperationsLeads submission teams or regulatory sub-teams to ensure timely filings that meet product launch deadlines for:Marketing applications: NDA/BLA/MAA/ExtensionsClinical trial applications: IND/CTA/CTR submissions aligned with trial initiation milestonesResponsible for developing and maintaining the core global dossier; collaborating with regional leads on region-specific submissionsLeads development and implementation of expedited regulatory pathways, including:Development programs: Fast Track Designation (FTD), Breakthrough Therapy Designation (BTD), Regenerative Medicine Advanced Therapy (RMAT), PRIMEReview processes: Priority Review, Project Orbis, Real-Time Oncology Review (RTOR), Conditional ApprovalExecutes operational and compliance activities for assigned deliverables:Generates submission content plansTracks submission Progress and milestonesLeverages cross-functional teams and alliance partners as neededAbout youExperienceBS/BA degree in a scientific discipline or MSc in Biology, Life Science, or related field is required with at least 8 years of relevant pharmaceutical/biotechnology industry experience, including at least 6 years of relevant Regulatory Affairs experience in the oncology therapeutic area ORAdvanced degree (PharmD, PhD, MD or DVM) with at least 4 years of regulatory or relevant pharmaceutical/biotechnology industry experience required include at least 2 years of relevant Regulatory Affairs experience in the oncology therapeutic area.Technical SkillsUnderstanding of clinical development of drugs and/or innovative biologics products is preferred.Demonstrated experience with driving the preparation of regulatory documents (e.g. (s)BLA/(s)NDA/ MAA, INDs/CTAs, Health Authority meeting briefing documents) and negotiating with a national/regional Health Authority is desirable.Experience working in and strong knowledge of electronic document management systems (e.g. Veeva Vault RIM, Plai) is desirableExperience working with AI platforms when establishing regulatory environment, current industry best practices, etc. is a plus.Soft SkillsEffective communication skills, specifically strong oral and written presentation skills.Sensitivity for a multicultural/multinational environmentEmerging business acumen, leadership, influencing and negotiation skills.Ability to use appropriate interpersonal styles and techniques to build internal and external networks and lead discussions with internal and external stakeholders.Why Choose UsBring the miracles of science to life alongside a supportive, futurefocused 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 drugdevelopment quicker and more effective.Sanofi Inc. and its U.S. affiliates are Equal Opportunity andAffirmative 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.All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.#J-18808-Ljbffr

Skills:
Artificial Intelligence (AI), Best Practices, Biology, Biotech and Pharmaceutical, Business Plan, Business Skills, Click Through Rate (CTR), Communication Skills, Compensation Management, Compensation and Benefits, Cross-Functional, Document Management, Documentation, Drug Development, Drug Discovery, Drug Products, Employee Benefits, Genetics, Healthcare, Healthcare Quality, International Health, Interpersonal Skills, Investigational New Drug (IND), Leadership, Marketing Authorization Application (MAA), Marketing Software, Medical Products, Medicine, Multicultural, Negotiation Skills, Oncology, Policy Implementation, Power Amplifier, Presentation/Verbal Skills, Product Development, Product Planning, Product Strategy, Product/Service Launch, Regulations, Regulatory Submissions, Research & Development (R&D), Team Lead/Manager, Time Management, Vaccination, Veterinary Medicine, Writing Skills

About the Company:
Eacademy Sanofi