Urwah Admin

Sanofi

<div>Job title: iCare Advanced Analytics and AI, Product Line Owner
Location: Cambridge, MA / Morristown, NJ
About the Job
Ready to push the limits of what&rsquo;s possible? Join Sanofi in one of our corporate functions and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world.
At Sanofi, we&rsquo;re committed to providing the next-generation healthcare that patients and customers need. It&rsquo;s about harnessing data insights and leveraging AI responsibly to search deeper and solve healthcare challenges and unmet needs sooner than ever before.
Join the Digital Global Business Unit focused on delivering the best-in-class personalized digital experience to customers and patients powered by data-driven decisions. This role will focus specifically on the digital experience of consumers and/or patients who could benefit from Sanofi specialty therapies. As part of the Patient/Consumer Advanced Analytics &amp; AI team, you will be accountable to provide the data, systems and analytical tools to identify and resolve issues encountered by consumers/patients on their health journey.
You&rsquo;ll define the product strategy, lead a global team, and partner with cross-functional teams spanning Patient Support Services (PSS), Data Engineering, Data Science and more.
The ideal candidate brings a deep background in Reporting &amp; Analytics, GenAI/Agentic AI and Product leadership and possesses a passion for innovation, clear communication, and driving measurable business impact.
This is a highly visible role that requires strong strategic thinking, stakeholder influence, and the ability to translate complex data into clear, compelling narratives for both business and technical audiences.
As the iCare Advanced Analytics (AA) &amp; AI Product Line Owner you will lead Sanofi&rsquo;s Patient Support Services Digital Advanced Analytics &amp; AI portfolio globally with a focus on the US. That includes:<ul><li>
Enabling Patient Support Services reporting and ad-hoc analysis, providing insights to leadership for all relevant specialty therapies on patient journey bottlenecks</li><li>
Scaling iCare Analytics outside of the US with a focus on measuring impact</li><li>
Leading the transition from Business Intelligence to GenAI/Talk-To-Data</li><li>
Governing the Snowflake data warehouse containing all relevant datasets associated with our patient support ecosystem (Aggregated Patient Files, Patient Relationship Management (PRM) and connected Digital Therapeutic applications (Dtx)) which requires the utmost integrity in governing sensitive privacy related information</li><li>
Right sizing and managing a team of internal and external resources</li><li>
Identifying and incorporating AA &amp; AI innovations to remove patient journey hurdles</li></ul>
About Sanofi:
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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&rsquo;s lives.
Main Responsibilities:
Product Strategy &amp; Ownership<ul><li>
Define and execute the strategy for iCare AA &amp; AI products, in alignment with GBU/PSS and digital priorities</li><li>
Own the end-to-end product lifecycle: vision, design, build, rollout, operations, and continuous improvement</li><li>
Develop and manage the product roadmap, budgets, resource allocation, and localization across brands and markets</li><li>
Define and track success metrics for all iCare AA &amp; AI products</li><li>
Ensure value realization through performance tracking and product evolution</li></ul>
Cross-Functional Leadership<ul><li>
Drive stakeholder alignment and communication by translating complex technical concepts into compelling, business-relevant narratives for executive leadership, GBU/PSS partners, and cross-functional stakeholders</li><li>
Serve as a visible champion of iCare analytics and AI initiatives across the organization, influencing strategy, securing buy-in, and presenting product vision, roadmap, and outcomes to senior audiences</li><li>
Lead a team of product owners, data analysts and collaborate closely with GTMC, brand teams, market stakeholders, and external partners</li><li>
Drive structured ways of working to maximize value delivery and operational efficiency</li></ul>
Compliant Analytics &amp; AI Product Development<ul><li>
Design and deploy AI and analytics products that enhance insights for Patient Support Services</li><li>
Collaborate on AI/analytics strategy, use case identification, and platform/tool development with GTMC Data &amp; Insights</li></ul><ul><li>
Oversee the automation of reporting workflows to improve speed, scalability, and accuracy</li><li>
Ensure compliance with relevant regulatory standards in all reporting and data activities</li><li>
Implement quality control practices to maintain high data reliability and integrity.</li><li>
Ensure ethical use of patient and caregiver data in compliance with privacy regulations (e.g., GDPR, HIPAA), in collaboration with Legal and Compliance.</li></ul>
Continuous Improvement<ul><li>
Drive innovation and business transformation by fostering a culture of problem-solving, experimentation &amp; agility</li><li>
Continuously evaluate new technologies and methods to improve product performance and business outcomes</li><li>
Push on conventional wisdom with a strong point of view; take the initiative and offer creative solutions</li></ul>
About You<ul><li>
Core (technical) requirements:<ul><li>
Bachelor&rsquo;s degree in Computer Science, Information Systems, Software Engineering, Business/Data Analytics or similar field</li><li>
10+ years of experience working in Reporting/Analytics</li><li>
3+ years of people leadership experience in cross-functional and global settings</li><li>
Proven track record of leading successful AI/analytics product delivery in complex organizations</li><li>
Ability to rapidly understand key business processes and their corresponding data flows</li><li>
Proficiency in reading, evaluating SQL logic and corresponding output</li><li>
Knowledge of KPIs, hierarchies, and the understanding of data relationships</li><li>
Understanding of Snowflake data warehouse architecture and capabilities</li><li>
Experience in driving the use of AI/Gen-AI for efficiency gains (quality, speed of delivery) as well as leveraging Gen-AI on structured data (talk-to-data)<ul><li>
Experience in prompt engineering</li><li>
Experience developing semantic layers</li><li>
Experience building agentic frameworks</li></ul></li><li>
Understanding of US healthcare data / claims data</li></ul></li><li>
Core soft skills requirements:<ul><li>
Track-record of problem-solving &amp; overcoming roadblocks in a complex environment, with a &ldquo;get things done&rdquo; mindset</li><li>
Strong cross-functional leadership &amp; influencing skills including an ability to work efficiently cross-functionally with:<ul><li>
Internal/external data engineers to test outcomes and recommend enhancements</li><li>
Business stakeholders to understand business priorities and pull through digital solutions</li></ul></li><li>
Proven ability to build credibility and trust with business stakeholders:<ul><li>
Translating technical complexity into business value and strategic impact</li><li>
Delivering on commitments and managing stakeholder expectations proactively</li><li>
Demonstrating business acumen and understanding of commercial/medical priorities</li></ul></li><li>
Strong verbal and written communication skills</li></ul></li><li>
Preferred experience:<ul><li>
15+ years of experience working in Reporting/Analytics</li><li>
5+ years of people leadership experience in cross-functional and global settings</li><li>
Pharmaceutical Patient Support Services experience, e.g., knowledge of healthcare data privacy &amp; compliance regulations, PRMs</li><li>
Experience in Agile development processes and DevOps methodology / principals</li><li>
Proficiency in segmentation testing, A/B testing methodologies, and experimental design for impact assessments</li></ul></li></ul> 
Why Choose Us?<ul><li>
Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>
Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.</li><li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>
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&rsquo; gender-neutral parental leave.</li></ul>
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.
#GD-SA
 
#LI-SA 
#LI-Onsite 
#vhd
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.</div>

iCare Advanced Analytics and AI, Product Line Owner

<div>Job title: Senior Product Manager, Consumer Marketing, Rare Hematology
Location: Cambridge, MA
About the job
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you&rsquo;ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.
As Senior Product Manager, within the Rare Hematology team, you&rsquo;ll support key elements of the U.S. consumer marketing strategy and execution for WAYRILZ, the first BTK inhibitor for Immune Thrombocytopenia (ITP), FDA approved in August 2025. This role will serve as a key bridge between strategic planning and tactical execution &ndash; with a focus on omnichannel campaign delivery, digital marketing optimization and patient engagement initiatives.
This is an opportunity for an emerging marketer to deepen cross-functional collaboration, develop digital fluency, and make meaningful contributions to a high-impact, priority launch asset for the U.S. Rare Blood Disorders Franchise and Sanofi Specialty Care. This role reports to the Director of Consumer Marketing, Rare Hematology and will be based in Cambridge, MA.
About Sanofi
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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&rsquo;s lives.
Main Responsibilities:
Strategic Contribution &amp; Campaign Execution<ul><li>
Contribute to the U.S. commercial strategy for WAYRILZ by supporting patient marketing efforts as part of the consumer marketing team, working alongside the Director and Associate Director, and in partnership with the broader Rare Hematology marketing team</li><li>
Lead day-to-day execution of omnichannel patient campaigns across digital and traditional channels, including website content, email marketing, social media, and print materials - from content creation through legal/regulatory approval, field training, and launch</li><li>
Monitor campaign performance, market research insights, and patient feedback to identify optimization opportunities and inform future consumer marketing strategies</li></ul>
Patient Ambassador Program &amp; Engagement<ul><li>
Serve as the primary owner of the ITP patient ambassador program, managing end-to-end logistics in partnership with our patient ambassador logistics agency, including ambassador recruitment, training, scheduling, event coordination, and ongoing engagement</li><li>
Partner closely with legal, regulatory and compliance teams to ensure all ambassador activities adhere to FDA guidelines, PhRMA Code, and company policies</li><li>
Develop compelling patient storytelling content (testimonials, videos, social media, case studies) that educates, empowers, and builds trust with the ITP community while maintaining full regulatory compliance</li></ul>
Cross-Functional Partnership &amp; Agency Management<ul><li>
Build strong collaborative relationships across patient support services, advocacy, digital, GTMC, market research and field teams to ensure alignment with WAYRILZ patient strategy and uncover actionable insights</li><li>
Work closely with agency partners to manage project timelines, deliverables, budgets, and quality standards&mdash;ensuring work stays on strategy, on time, and within budget</li><li>
Coordinate cross-functional review processes (MLR) and manage day-to-day operational logistics for print fulfillment, patient events, and field enablement materials</li></ul>
About You
Required Qualifications:<ul><li>
4&ndash;6 years of progressive experience in pharmaceutical marketing, digital strategy, consumer healthcare, or agency account management</li><li>
Strong understanding of omnichannel marketing and digital patient engagement tactics (web, CRM/email, social media, paid media, etc.)</li><li>
Experience working in regulated industries with demonstrated knowledge of legal/regulatory review processes and promotional compliance requirements</li><li>
Proven ability to manage multiple complex projects simultaneously with strong attention to detail, prioritization skills, and accountability for results</li><li>
Excellent cross-functional collaboration and communication skills, with the ability to influence and build relationships across diverse stakeholder groups</li><li>
Self-starter who can work independently to develop clear action plans, manage timelines, set objectives, and oversee budgets</li><li>
Willingness to travel approximately 15&ndash;20%</li></ul>
Preferred Qualifications:<ul><li>
Experience managing patient or brand ambassador programs, including logistics, compliance oversight, and content development</li><li>
Background in rare disease, specialty care, or launch marketing</li><li>
Familiarity with pharmaceutical digital platforms (e.g., Veeva Vault PromoMats, iCare, Salesforce Marketing Cloud, or similar)</li><li>
Event planning and coordination experience</li><li>
Demonstrated patient-centric mindset and comfort working directly with patient communities in a compliant, empathetic manner</li><li>
Growth mindset with eagerness to learn and adapt in a fast-paced, high-visibility launch environment</li></ul>
Why Choose Us?<ul><li>
Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>
Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.</li><li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>
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&rsquo; gender-neutral parental leave.</li></ul>
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.
#GD-SG 
#LI-GZ 
#LI-Onsite 
#vhd
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.</div>

Senior Product Manager, Consumer Marketing, Rare Hematology

<div>Job title: Product Owner - R&amp;D Authoring and Content Reuse<ul><li>
Location: Morristown, NJ</li></ul>
About the Job
As Product Owner - R&amp;D Authoring and Content Reuse within our Digital team, you will join the digital engine driving Sanofi's transformation, where AI, automation, and bold experimentation power faster science and smarter decisions. Here, you'll help build the first biopharma company powered by AI at scale.
In this role, you will design and deliver enterprise-scale AI-enabled document authoring products supporting R&amp;D authoring processes. Acting at the interface between R&amp;D and technical teams, you will ensure solutions effectively meet Sanofi's needs, drive adoption, and directly impact regulatory submission timelines &mdash; accelerating drug approvals by months.
Join the digital engine driving Sanofi&rsquo;s transformation - where AI, automation, and bold experimentation power faster science and smarter decisions. Here, you&rsquo;ll help build the first biopharma company powered by AI at scale.
About Sanofi
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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&rsquo;s lives.
Main responsibilities
As a Product Owner, you will drive enterprise-wide transformation across the following areas:<ul><li>
Product Roadmap: Co-define and execute a multi-year product strategy with the Product Line Owner. Manage product budget and drive ROI through strategic vendor partnerships and technology investments.</li><li>
Requirements Management: Gather, analyze, prioritize, and translate user requirements into clear user stories and acceptance criteria.</li><li>
Cross-team Collaboration: Coordinate multiple agile streams, vendors, and internal digital capabilities. Partner with R&amp;D, Digital, and external teams, and contribute to cross-functional governance across R&amp;D.</li><li>
Backlog Management: Maintain a prioritized product backlog, ensure development teams have clear requirements, and sustain execution velocity.</li><li>
Quality: Ensure adherence to regulatory requirements. Lead validation strategies for AI systems in GxP environments, setting industry best practices.</li><li>
Training &amp; Adoption: Coordinate user training with relevant stakeholders and support adoption of new features.</li><li>
Value Realization: Deliver measurable impact on R&amp;D metrics &mdash; including reduced document creation time and improved content quality. Track usage metrics, user satisfaction, and adoption.</li></ul>
About you
Education<ul><li>
Bachelor's degree in life sciences, informatics, Computer Science, Technology or related field, (Master's or PhD is a plus)</li></ul>
Experience<ul><li>
5+ years of experience in product ownership or Product management roles, delivering enterprise-scale solutions</li><li>
Familiarity with document authoring processes</li><li>
Experience managing budgets and complex vendor relationships</li></ul>
Soft and Technical skills:<ul><li>
Strong prioritization and stakeholder management skills with a data-driven approach</li><li>
Proficiency in agile methodologies (Scrum, Kanban, SAFe) and associated tools</li><li>
Ability to build consensus while maintaining a clear product vision</li><li>
Excellent communication and collaboration skills across all organizational levels</li><li>
Experience with Jira and Confluence</li><li>
Comfortable navigating ambiguity, adapting strategy, and delivering results in fast-paced environments</li><li>
Ability to reimagine business processes and technology solutions using disruptive technologies</li><li>
Demonstrated drive for change management and technology adoption</li><li>
Strong learning agility with curiosity for emerging technologies &mdash; able to quickly grasp new concepts, regulatory domains, and innovative ways of working</li></ul>
Nice to have:<ul><li>
PSPO or equivalent certification</li><li>
Experience in highly regulated GxP environments</li></ul>
Languages<ul><li>
English (fluent)</li></ul> 
Why Choose Us:<ul><li>
Bring the miracles of science to life alongside a supportive, futurefocused team.</li><li>
Discover endless opportunities to grow your talent and drive your 
career, whether it&rsquo;s through a promotion or lateral move, at home or 
internationally.</li><li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>
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&rsquo; gender-neutral parental leave.</li><li>
Join the digital force behind Sanofi&rsquo;s AI-powered pipeline, where Expert, Generative, and Snackable AI accelerate the discovery, development and delivery of breakthrough treatments to patients.</li><li>
Help reduce time from discovery to commercialization, delivering life-changing medicines to patients faster than ever.</li><li>
Join a workplace where diversity, equity, and inclusion are at the core, with Employee 
Resource Groups and leadership programs that celebrate every voice.</li></ul>
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.
#GD-SA
#LI-SA
#vhd
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.</div>

Product Owner - R&D Authoring and Content Reuse

<div>
 
 About Sanofi
 
 
 
 We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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&rsquo;s lives.
 
 
 
 About The Job
 
 
 
 <ul>
 <li>
 Define, implement and maintain the Partner Market PV business model under the direction of the Multi-Country Safety Head ((M)-CSH). ensure an effective oversight and management of the Partner Market Service Providers (PMSP) across the MCO/region including regular meetings with the PMSPs, monitoring compliance with the PV Agreements (PVAs) and maintenance of the PVA.
 </li>
 <li>
 Ensure the implementation of PV in assigned territories, acting as the interface between PSPV, the (M)CSH and the PMSPs.
 </li>
 <li>
 Transversal coordination: ensures PV training, processes and tools are in place with the PMSPs, ensures that they are compliant with PV standards and are harmonized across countries. The Partner Market PV Manager shall identify areas of risk and escalate and work with stakeholders to resolve. Promote and deploy initiatives aimed at harmonizing and promoting best practices across PMSPs within assigned territory (if applicable). In addition, when appropriate, he/she may need to work collaboratively with the Global PSPV SMEs in developing process-related solutions oriented at the PMSPs as well as interacting closely with other PSPV functions to contribute to the appropriate management of the Sanofi PV system.
 </li>
 <li>
 Is the contact point between PMSPs and the Global PV teams, and performs other activities which require a coordination role as new process implementation, communication to partners, implementation of additional Risk Minimization Measures and its tracking, contribution to the PSMF, supports Inspection and Audit activities etc.
 </li>
 <li>
 Work collaboratively with other Sanofi functions contributing to the success of the PMSPs collaboration.
 </li>
 <li>
 Serves as back-up for Partner Market PV Managers in other territories/Regions as required
 
 
 </li>
 </ul>
 
 Key Accountabilities
 
 
 
 <ul>
 <li>
 Manage great customer experience: Acts as the contact point/interface between PSPV/internal and external stakeholders (i.e Partner Market Service Providers)
 </li>
 <li>
 Oversees the Partner Market Service Providers ensuring the maintenance and compliance with the PVAs. Ensures all Partner Market Service Providers meet KPIs set by PSPV, and oversee compliance of partners with applicable regulations.
 </li>
 <li>
 Routine management and support of the PV aspects of the Partner Market Services Providers, including support for audit and inspection.
 </li>
 <li>
 Participates in the Due diligence activities to select the service provider for PV activities when applicable.
 </li>
 <li>
 Follows up overall project implementation plan for new Partner Markets implementation, which involves the transition of PV activities to partners in countries in scope and ensure no noncompliance.
 </li>
 <li>
 Keeps the Multi-Country Safety Head informed on the status of the allocated Partnerships escalating issues as needed.
 </li>
 <li>
 Ensures the Multi-Country Safety Head has the comprehensive oversight and management of all the partnerships for the delegated PV activities including monitoring and enforcement of Partners compliance with the PV Agreements.
 </li>
 <li>
 In collaboration with other Partner Market PV Managers: Coordinates the implementation of the PV activities consistently across PMSPs in the assigned territories when applicable. Ensures back-up functions are in place across MCO/Regions as applicable.
 </li>
 <li>
 Is in charge of the monitoring of the budget of PMSP activities, in collaboration with the (M)-CSH.
 
 
 </li>
 </ul>
 
 Education
 
 
 
 
 About you
 
 
 
 <ul>
 <li>
 MD, Pharmacist, PhD or master&rsquo;s degree in Human Health Sciences
 
 
 </li>
 </ul>
 
 Experience &amp; Knowledge
 
 
 
 <ul>
 <li>
 Minimum 4 years&rsquo; experience in managing Pharmacovigilance activities in close collaboration with key departments (Medical Affairs, Regulatory, Clinical, Quality Assurance, etc.) or equivalent experience.
 </li>
 <li>
 Experience working in multinational environment, across diverse cultures
 </li>
 <li>
 Experience with PV agreements and or PV partnerships and partner/vendor relations
 </li>
 <li>
 Experience in transversal projects
 </li>
 <li>
 Knowledge of other languages, Fluency in French is advantageous.
 </li>
 <li>
 Country PV experience is an asset.
 </li>
 <li>
 Experience with Clinical Safety related activities can be a plus
 </li>
 <li>
 Knowledge of other languages. Fluency in French is advantageous
 </li>
 <li>
 Project management experience.
 
 
 </li>
 </ul>
 
 Competencies
 
 
 
 <ul>
 <li>
 Excellent organizational and planning capabilities
 </li>
 <li>
 Strong negotiation skills
 </li>
 <li>
 Strong interpersonal skills
 </li>
 <li>
 Strong leadership competencies
 </li>
 <li>
 Team player
 </li>
 <li>
 Fluency in English (both oral and written, including technical terminology) and communication skills (oral/written)
 </li>
 <li>
 Inter-cultural skills/ability to work across cultures.
 </li>
 <li>
 Demonstrate problem solving skills, sense of urgency, especially with respect to enforcing safety rules and global procedures as described in QDs, Operational Manuals and Guidance documents. Capacity to work under pressure
 
 
 </li>
 </ul>
 
 Take The Lead Values
 
 
 
 <ul>
 <li>
 Aim Higher - Focus on what matters, set high standards and move with urgency, learning from setbacks as we go to achieve higher performance.
 </li>
 <li>
 Act for patients - Never compromise on integrity, eliminate barriers, and partner with others to go faster and further for patients.
 </li>
 <li>
 Be Bold - Take thoughtful risks, seize opportunities and think beyond what&rsquo;s possible to accelerate our science and drive compelling growth.
 </li>
 <li>
 Lead Together - Build trust and collaborate openly on our shared goals, celebrate collective wins and foster a sense of belonging.
 
 
 </li>
 </ul>
 
 Why choose us?
 
 
 
 <ul>
 <li>
 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.
 </li>
 <li>
 Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.
 </li>
 <li>
 Help improve the lives of millions of people globally by making drug development quicker and more effective.
 </li>
 <li>
 Enjoy opportunities to collaborate beyond your area of expertise, working with diverse teams across science, clinical, and digital fields to spark new ideas and drive breakthroughs.
 </li>
 <li>
 Accelerate your professional development with structured career paths designed for both scientific and leadership advancement. Grow in ways you never imagined through bold moves that stretch your potential, cross moves into other business areas, and short-term gigs that build your scientific expertise.
 </li>
 <li>
 Join a workplace where diversity, equity, and inclusion are at the core, with Employee Resource Groups and leadership programs that celebrate every voice.
 </li>
 <li>
 Achieve genuine work-life balance in a supportive R&amp;D environment.
 </li>
 <li>
 Enjoy outstanding benefits, including flexible working options, comprehensive healthcare, and well-being programs designed to help you thrive.
 
 
 </li>
 </ul>
 null
</div>

Partner Market PV Manager – Sub Saharan Africa

<div>Job title: Medical Science Liaison &ndash; Oncology<ul><li>
Location: Riyadh, Saudi Arabia</li></ul>
About the job
As Medical Science Liaison &ndash; Oncology within our Specialty Care team, you'll serve as a trusted scientific partner to key oncology stakeholders, bridging cutting-edge clinical insights with real-world medical practice. Ready to get started?
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you'll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.
About Sanofi
We're an R&amp;D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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<ul><li>
Build and maintain trusted scientific relationships with Key Opinion Leaders (KOLs) and healthcare professionals to advance understanding of oncology therapy areas, including Multiple Myeloma.</li><li>
Provide accurate, balanced, and timely medical information to healthcare professionals and decision-makers in response to clinical inquiries.</li><li>
Collaborate with Medical Affairs and clinical teams to support Real-World Evidence studies, Phase IV clinical projects, Investigator-Sponsored Studies (ISS), and site selection for clinical trials.</li><li>
Serve as a scientific resource for the commercial team, supporting objection handling and acting as a therapy area expert.</li><li>
Actively represent Sanofi at key medical and scientific conferences, staffing medical information booths and gathering competitive intelligence.</li><li>
Receive, report, and transmit adverse events in line with company pharmacovigilance procedures, and ensure Risk Management Plan implementation.</li><li>
Uphold compliance, ethical leadership, and safety standards in all field activities.</li></ul>
About you<ul><li>
Experience: Prior 3 years of experience in Medical Affairs within the pharmaceutical industry, with a background in Oncology and/or Multiple Myeloma being a strong advantage.</li><li>
Soft and technical skills: Strong scientific communication skills with the ability to engage KOLs and cross-functional stakeholders at all levels; knowledge of clinical research methodology and GCP; business acumen and self-motivation; collaborative team player with strong planning and decision-making abilities.</li><li>
Education: University degree in life sciences; MD, PhD, or PharmD preferred.</li><li>
Languages: Fluency in Arabic and English required.</li></ul>
Why choose us?<ul><li>
Join the team transforming care for patients with some of the highest unmet needs &mdash; including rare cancers and immune-mediated diseases &mdash; and be part of delivering hope where it matters most.</li><li>
Work at the intersection of science and patient impact, engaging directly with leading oncology KOLs and shaping the future of cancer care in the region.</li><li>
Grow your career in a cross-functional environment with access to global Medical Affairs expertise, international mobility, and continuous development opportunities.</li><li>
Be part of a company that invests in you &mdash; with structured career paths, mentoring, and a culture that values bold thinking and scientific excellence.</li><li>
Thrive in an inclusive, purpose-driven workplace where your contributions directly improve patients' lives across Saudi Arabia and beyond.</li><li>
Enjoy a comprehensive rewards package including healthcare benefits and flexible working arrangements.</li></ul>
Pursue Progress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what's never-been-done-before. You'll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people's lives? Let's Pursue Progress and Discover Extraordinary &ndash; together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
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Medical Science Liaison Oncology

<div>
 
 Job Title:
 
 Media Content Creator (Brand &amp; 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&rsquo;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&mdash;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&rsquo;s AICE team and help reimagine how we engage healthcare professionals through data, intelligence, and automation. In this role, you&rsquo;ll directly shape how media content is created, scaled, and activated globally&mdash;contributing to a faster, smarter, and more AI-enabled marketing model that drives measurable impact.
 
 
 
 About Sanofi
 
 
 
 We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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&rsquo;s lives.
 
 
 
 Main Responsibilities
 
 
 
 
 Content Development &amp; Adaptation
 
 
 
 <ul>
 <li>
 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.
 </li>
 <li>
 Create high-impact promotional assets (banners, social units, article adaptations, long-form HCP content, educational videos) aligned to approved messaging, claims, and brand strategy.
 </li>
 <li>
 Translate global strategy and claims into concise, compelling, and compliant promotional content tailored to HCP audiences across markets.
 </li>
 <li>
 Collaborate closely with Studio designers, writers, and media partners to ensure channel-fit content, optimizing copy length, visual execution, and platform requirements.
 </li>
 <li>
 Ensure all assets reflect approved claims, accurate scientific data, and brand tone while aligning with local cultural and regulatory nuances.
 
 
 </li>
 </ul>
 
 Market Collaboration &amp; Execution
 
 
 
 <ul>
 <li>
 Partner with the Market Integration Partner and local market teams to ensure content aligns with local regulatory requirements, media plans, and platform specifications.
 </li>
 <li>
 Serve as the primary point of contact for markets on content localization, versioning, media adaptations, and compliance alignment.
 </li>
 <li>
 Coordinate end-to-end delivery of promotional assets, ensuring correct formatting, timely handoffs to media agencies, and on-time deployment.
 </li>
 <li>
 Capture in-market feedback and performance insights to support ongoing optimization of non-personalized promotional (NPP) content.
 
 
 </li>
 </ul>
 
 Compliance &amp; MLR Readiness
 
 
 
 <ul>
 <li>
 Prepare and submit all promotional assets for MLR review, ensuring strict adherence to local regulations and internal standards.
 </li>
 <li>
 Partner with MLR reviewers to address questions and revisions efficiently, maintaining accuracy across claims, references, annotations, and visual executions.
 </li>
 <li>
 Ensure all assets&mdash;including derivatives and localized versions&mdash;are fully traceable, audit-ready, and properly documented in systems such as Veeva PromoMats.
 </li>
 <li>
 Maintain consistent documentation and version control across markets and media formats.
 
 
 </li>
 </ul>
 
 Operational Support &amp; Continuous Improvement
 
 
 
 <ul>
 <li>
 Manage the full content lifecycle from creation through approval, localization, tagging, archiving, and reuse.
 </li>
 <li>
 Ensure structured metadata and proper tagging to support media activation, version control, and content reuse.
 </li>
 <li>
 Support reporting and tracking across content timelines, approvals, and deployments to provide transparency for Studio, media, and market teams.
 </li>
 <li>
 Identify opportunities to standardize templates, streamline workflows, and improve efficiency, including leveraging automation and modular content approaches.
 </li>
 <li>
 Contribute to playbooks, best practices, and shared standards that elevate quality, consistency, and scalability of media content across AICE.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 
 About You
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Marketing, Communications, English, Journalism, or a related field.
 </li>
 <li>
 4+ years of experience in pharmaceutical promotional content development.
 </li>
 <li>
 Strong copywriting and editorial skills, with a proven ability to translate scientific and medical information into clear, engaging promotional content.
 </li>
 <li>
 Deep understanding of pharmaceutical MLR processes and regulatory compliance standards.
 </li>
 <li>
 Experience working with Veeva PromoMats or similar content management and approval systems.
 </li>
 <li>
 Strong project management skills with the ability to manage multiple workstreams simultaneously.
 </li>
 <li>
 Excellent collaboration and communication skills across creative, regulatory, media, and market teams.
 </li>
 <li>
 Fluency in English required; proficiency in French is a plus.
 
 
 </li>
 </ul>
 
 Why Choose Us?
 
 
 
 <ul>
 <li>
 Bring the miracles of science to life alongside a supportive, future-focused team.
 </li>
 <li>
 Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.
 </li>
 <li>
 Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
 </li>
 <li>
 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&rsquo; gender-neutral parental leave.
 
 
 </li>
 </ul>
 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.
 
 
 #GD-SG
 
 
 #vhd
 
 
 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.
 
 
</div>

Media Content Creator (Brand & Media Storyteller)

<div>Job title: Area Business Manager, Pulmonology - Seattle, WA<ul><li>
Location: Seattle, WA</li></ul>
About the job
Sanofi has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases, oncology, immunology and multiple sclerosis, we are dedicated to making a positive impact on the lives of the patients and families we serve. Sanofi portfolio of transformative therapies, which are marketed in countries around the world, represent groundbreaking and life-saving advances in medicine.
The Area Business Manager (ABM) is responsible for engaging Pulmonologists, and other key customers within an assigned geography and presenting clinically focused selling messages to create and grow revenue and to consistently deliver product goals related to asthma and COPD indications. The ABM will demonstrate initiative, drive, independence, and take ownership for meeting and exceeding individual business goals. This will be accomplished by driving performance and delivering results in a compliant manner with a high degree of integrity strictly following all Sanofi Specialty Care US policies and in compliance with all policies and procedures governing the promotion of pharmaceutical/biological products in the US.
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&amp;D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, you&rsquo;ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.
About Sanofi:
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; 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&rsquo;s lives.
Main Responsibilities:<ul><li>
Engage Pulmonology customers within assigned geographical territory and deliver clinically focused message to introduce, launch, grow brand-share and revenue and to consistently deliver on product goals for asthma and COPD indications.</li><li>
Collaborate and coordinate with other key field-based stakeholders such as Regeneron Sales Professional counterparts, Medical Science Liaisons, Field Reimbursement and Market Access teammates, Thought Leader Liaisons, and others in their territory to proactively address customer needs, identify market dynamics and trends, develop strategies which support brand and corporate objectives, and ensure optimal account success within their assigned geography.</li><li>
Develop strong working relationships with Pulmonology experts in assigned geography as well as biologic coordinators, office staff and other important health care personnel and key patient advocacy support groups as directed.</li><li>
Drive results by identifying key opportunities and developing strategic business plans to generate product utilization and grow territory business.</li><li>
Plan, organize, and execute local promotional speaker programs and activities.</li><li>
Maximize budget allocated to the geographic territory to support execution of strategies and tactics and generate/grow the business.</li><li>
Participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</li><li>
Own business opportunities within respective geographic area, which includes coordination and calling upon large group practices and other key targets to drive overall product results.</li><li>
Establish relationship with thought leaders in assigned territory. Primary objective is to drive industry leading customer value.</li></ul>
About You
Basic Qualifications:<ul><li>
Bachelor&rsquo;s degree from an accredited four-year college or university.</li><li>
3+ years of pharmaceutical, biotech, or medical device sales experience.</li><li>
Demonstrated ability to learn and apply technical and scientific product-related information.</li><li>
Ability to travel to meetings/trainings/programs as necessary - additional travel may be required within the assigned territory.</li><li>
Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines.</li><li>
Ability to operate as a &ldquo;team player&rdquo; in cooperation with collaboration partners and internal colleagues to reach common goals.</li><li>
Valid Driver&rsquo;s License.</li></ul>
Preferred Qualifications:<ul><li>
2+ years selling sub-cutaneous self-injectable (or office administered IV) biologics in a complex and competitive market.</li><li>
2+ years selling experience in asthma and/or COPD, or other immunology disorders such as atopic dermatitis, psoriasis, multiple sclerosis, Crohn&rsquo;s disease, or ulcerative colitis strongly preferred.</li><li>
2+ years selling experience calling on Pulmonologists or Respiratory sales experience (COPD, ENT or alike) preferred.</li><li>
Launch experience in specialty care and biologics strongly preferred.</li><li>
Alliance/matrix partnership experience strongly preferred.</li><li>
Demonstrate advanced clinically based selling skills.</li><li>
Results oriented with a proven track record of success with product launches.</li><li>
Experience with in-servicing and training office staff, nurses and office managers.</li><li>
Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends.</li><li>
Highly organized with strong account management skills.</li></ul>
Candidates must complete all fleet safety training and must maintain an acceptable driving record regarding accidents and incidents.
Why Choose Us?<ul><li>
Bring the miracles of science to life alongside a supportive, future-focused team.</li><li>
Discover endless opportunities to grow your talent and drive your career, whether it&rsquo;s through a promotion or lateral move, at home or internationally.</li><li>
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.</li><li>
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&rsquo; gender-neutral parental leave.</li></ul>
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.
#GD-SG
 
#LI-GZ
#vhd
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.</div>

Area Business Manager, Pulmonology - Seattle, WA

Join Sanofi and explore 14   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.