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Sanofi EU
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  • Head of Commercial Strategy and Marketing Operations  

    - Morristown
    Job Title: Head of Commercial Strategy and Marketing Operations Locati... Read More
    Job Title: Head of Commercial Strategy and Marketing Operations Location: Morristown, NJ, Cambridge, MA About the Job Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, and AI-driven breakthroughs. In Vaccines, you'll help advance prevention on a global scale - and shape the future of immunization. You will be joining the US Vaccines team to lead the Commercial strategy and Marketing operations group working closely with local and global teams to define, orchestrate and implement portfolio and operational deliverables. Key collaborators include the US Vaccine Franchises, Sales teams across Health systems, Retail, portfolio sales, Operations, Digital, Customer Service and Global Brand Excellence. 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: Develop and Lead strategic projects across the portfolio working cross functionally across the organization related to short term and mid term priorities of the business. (e.g., competitive benchmarking, go-to-market evolution, resource allocation, channel & segment strategy) Lead annual strategic and operational planning exercise coordinating with US business franchises and North America Leadership team Drive marketing operations and excellence (includes partnering on omnichannel capabilities, annual sales meetings, congress/conventions, Control tower for priorities, other) Design and deliver cross brand initiatives working across marketing, sales, advocacy, medical. Examples include non-branded disease awareness materials (e.g., vaccine confidence campaign), articulating Sanofi competencies and positions on relevant public health topics. Develop the Sanofi Vaccines congress/conference strategy building a One Sanofi plan with medical. Attract, retain, develop and lead a team of marketers and marketing operations professionals , 5 + people, fostering talent development and capability building while role modeling Sanofi leadership behaviors. Engage with external stakeholders on behalf of Sanofi Vaccines. Member of the Marketing and Commercial Strategy Executive Leadership Team. About You Experience & Qualifications: Required: Bachelor's degree 8-10+ years of progressive experience in product/brand management, strategic marketing, commercial operations, or business development required, preferably within the pharmaceutical or biopharmaceutical industry Proven track record in developing and deploying business strategies across multiple customer channels (medical, health systems, specialty markets, wholesale/distribution, or public sector) Strong analytical and strategic thinking skills with demonstrated ability to drive business results Comprehensive understanding of the U.S. healthcare environment dynamics and market access landscape Experience leading, developing, and building high-performing teams Knowledge of U.S. commercial segments and channels Business operations and support experience Travel: Up to 25% travel required, domestic and international Hybrid work environment: 3 days per week in the office Preferred: Advanced degree (MBA, Master's equivalent) 3+ years of strategic consulting experience or strategy experience at a major pharmaceutical company in the U.S. Knowledge of the U.S. Vaccines sector and immunization landscape Experience in omnichannel marketing and digital engagement strategies 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 a 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 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. 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. Read Less
  • Media Content Creator (Brand & Media Storyteller)  

    - Morristown
    Job Title: Media Content Creator (Brand & Media Storyteller) Location:... Read More
    Job Title: Media Content Creator (Brand & Media Storyteller) Location: Morristown, NJ About the Job Join the team transforming how healthcare is delivered for chronic and specialty conditions worldwide. In General Medicines, you'll help drive meaningful outcomes in diabetes, transplant, and immunology - with the scale and urgency patients deserve. The AI-Driven Customer Engagement (AICE) team is transforming how Sanofi goes to market-redefining what modern marketing looks like. By blending human insight with AI, automation, and data, AICE is building a more intelligent, personalized, and efficient engagement model that accelerates impact across brands and markets. The Associate Director, Media Content Creation is responsible for developing, adapting, and operationalizing media-first promotional content across paid digital channels. This includes both short-form assets (display, banners, social units, video cut-downs) and long-form, high-value content such as articles, educational videos, and platform-native content developed in partnership with HCP media publishers. This is a hands-on, execution-focused role that operates without traditional agency support. The role translates global brand strategy and approved claims into high-quality, compliant content designed explicitly for digital media activation across local markets. You will work closely with the Market Integration Partner, Studio content talent, and local market teams to ensure content is accurate, compliant, culturally relevant, and optimized for media performance. Success in this role requires strong copywriting and content development skills, deep familiarity with pharmaceutical promotional standards, and the ability to balance creativity with precision and compliance in a fast-moving environment. Join Sanofi's AICE team and help reimagine how we engage healthcare professionals through data, intelligence, and automation. In this role, you'll directly shape how media content is created, scaled, and activated globally-contributing to a faster, smarter, and more AI-enabled marketing model that drives measurable impact. 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 Content Development & Adaptation Develop, adapt, and finalize media-first promotional content across paid digital channels, including display, social, video, HCP platforms, publisher partnerships, and long-form editorial content. Create high-impact promotional assets (banners, social units, article adaptations, long-form HCP content, educational videos) aligned to approved messaging, claims, and brand strategy. Translate global strategy and claims into concise, compelling, and compliant promotional content tailored to HCP audiences across markets. Collaborate closely with Studio designers, writers, and media partners to ensure channel-fit content, optimizing copy length, visual execution, and platform requirements. Ensure all assets reflect approved claims, accurate scientific data, and brand tone while aligning with local cultural and regulatory nuances. Market Collaboration & Execution Partner with the Market Integration Partner and local market teams to ensure content aligns with local regulatory requirements, media plans, and platform specifications. Serve as the primary point of contact for markets on content localization, versioning, media adaptations, and compliance alignment. Coordinate end-to-end delivery of promotional assets, ensuring correct formatting, timely handoffs to media agencies, and on-time deployment. Capture in-market feedback and performance insights to support ongoing optimization of non-personalized promotional (NPP) content. Compliance & MLR Readiness Prepare and submit all promotional assets for MLR review, ensuring strict adherence to local regulations and internal standards. Partner with MLR reviewers to address questions and revisions efficiently, maintaining accuracy across claims, references, annotations, and visual executions. Ensure all assets-including derivatives and localized versions-are fully traceable, audit-ready, and properly documented in systems such as Veeva PromoMats. Maintain consistent documentation and version control across markets and media formats. Operational Support & Continuous Improvement Manage the full content lifecycle from creation through approval, localization, tagging, archiving, and reuse. Ensure structured metadata and proper tagging to support media activation, version control, and content reuse. Support reporting and tracking across content timelines, approvals, and deployments to provide transparency for Studio, media, and market teams. Identify opportunities to standardize templates, streamline workflows, and improve efficiency, including leveraging automation and modular content approaches. Contribute to playbooks, best practices, and shared standards that elevate quality, consistency, and scalability of media content across AICE. About You Qualifications Bachelor's degree in Marketing, Communications, English, Journalism, or a related field. 4+ years of experience in pharmaceutical promotional content development. Strong copywriting and editorial skills, with a proven ability to translate scientific and medical information into clear, engaging promotional content. Deep understanding of pharmaceutical MLR processes and regulatory compliance standards. Experience working with Veeva PromoMats or similar content management and approval systems. Strong project management skills with the ability to manage multiple workstreams simultaneously. Excellent collaboration and communication skills across creative, regulatory, media, and market teams. Fluency in English required; proficiency in French is a plus. 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. 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. Read Less
  • Clinical Research Director  

    - Morristown
    Job Title: Clinical Research Director Location: Cambridge, MA, Morrist... Read More
    Job Title: Clinical Research Director 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. Reporting to the Global Project Head, the CRD leads clinical trial strategy of assigned program(s) within the clinical development team, including interactions with Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish the development strategy and execute the development plan. The clinical development team further develops a compound through life cycle management. 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 Establishes or adapts clinical development plan for the program(s) including discussions with clinical investigators, advisors and regulatory authorities and plans contingencies. Leads, supports and oversees the execution of clinical development and studies activities, including but not limiting to: Authors abbreviated protocol. Reviews the final protocol and protocol amendments. Reviews the Informed Consent Form, Written Subject Information and Trial Disclosure Form. Reviews the study specific committee charters. Leads study specific committees with operational support. Leads the clinical interpretation of study results, contributes to clinical study reports and clinical summaries. Provides effective clinical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine Participates and contributes to regulatory and safety documents and discussions Reviews and/or contributes clinical sections of the Investigator Brochure, IND/IMPD filings, DSUR, development risk management plans Contributes to the clinical sections of the NDA/CTD, Briefing packages for regulatory meetings, PSP/PIP Participates in Advisory Committee preparation Scientific data evaluation and authorship Authors clinical abstracts, presentations for conferences, and manuscripts, when appropriate Supports the planning of advisory board meeting. Presents and discusses development strategy and clinical study result with external investigators and advisory boards, as appropriate About You Job Requirements: MD degree or equivalent, with Medical Oncology fellowship. Hematology/Oncology fellowship or experience (4+ years) in Oncology Development Expertise in pharmaceutical medicine based on industry experience (3+ years) or academic clinical research experience (3+ years), Experience in clinical development, late-stage preferred Demonstrated ability to interact productively with external investigators Demonstrated ability to work with a multifunctional team to achieve project milestones Understanding of and willingness to meet applicable regulatory, quality and compliance standards 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. 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. Read Less

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