Sanofi

Content Manager

• Serve as the communications lead for the CX Center of Excellence (COE), owning the development and execution of internal communication strategies
• Be the lead subject matter expert representative for content strategy as part of our CX Foundation’s Community of Practice.
• Support the ongoing improvement of the CX COE SharePoint website to promote the goals, objectives, and value proposition of the Digital Consumer Experience team
• Develop the content frameworks to enable product teams to incorporate content best practices for multi-modal environments
• Advance organizational capability in agentic content experience by developing frameworks and guidance for designing content that functions effectively within AI-driven, autonomous, and conversational digital environments.
• Ensure CX content guidelines are maintained as living standards, with regular review cycles and clear governance processes
• Evolve standards, guidelines and toolkits for information architecture and taxonomy
• Plan and deliver training and workshops to upskill employees on content best practices

Digital Consumer Experience Content Strategist

Data Analyst

• Support the design, operationalization, and interpretation of measurement and insights capabilities of the DTC/P ecosystem
• Impact assessment of key digital direct consumer/patient experience products
• Collaborate with cross-functional teams to gather requirements, driving measurement and insight strategy for platform use cases
• Support and interpret measurement dashboards for key stakeholders to monitor real-time performance indicators and digital media engagement trends
• Help standardize and deliver digital products focusing on consumer/patient experience analytics and AI

DTC/P AA & AI, Data Analyst

Compliance

• Enables 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 projects
• Liaises with nonclinical, clinical, CMC, commercial, and other internal business partners in partnership with the GRL to enable successful regulatory outcomes
• Contributes to a harmonized, One Sanofi regulatory voice through participation in appropriate committees and forums, at the direction of the GRL
• Proactively 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 meetings
• Accountable 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 preparations
• May lead HA meetings and preparations as designated
• May serve as regional/local regulatory lead and point of contact with Health Authorities for projects/products within remit, as needed
• Leads submission teams or regulatory sub-teams to ensure timely filings that meet product launch deadlines for: Marketing applications: NDA/BLA/MAA/Extensions Clinical trial applications: IND/CTA/CTR submissions aligned with trial initiation milestones
• Responsible for developing and maintaining the core global dossier; collaborating with regional leads on region-specific submissions
• Leads development and implementation of expedited regulatory pathways, including: Development programs: Fast Track Designation (FTD), Breakthrough Therapy Designation (BTD), Regenerative Medicine Advanced Therapy (RMAT), PRIME Review processes: Priority Review, Project Orbis, Real-Time Oncology Review (RTOR), Conditional Approval
• Executes operational and compliance activities for assigned deliverables: Generates submission content plans Tracks submission progress and milestones Leverages cross-functional teams and alliance partners as needed

Global Regulatory Strategist

Manager

• Lead the end-to-end management of GRA's Quality Documentation system within QualiPSO (CMS), ensuring full compliance with Global Quality (GQ) standards and Medical Clinical Country Quality (MCCQ) -specific requirements
• Define, implement, and maintain the GRA QD System in alignment with GQ standards, MCCQ requirements, and applicable regulatory frameworks including 21 CFR Part 211 and GxP regulations
• Manage the complete document lifecycle — including creation, revision, approval, distribution, periodic review, and obsolescence — in accordance with QualiPSO procedures
• Oversee Document Change Request (DCR) management, ensuring changes driven by regulatory updates, process transformations, audit findings, or content improvements are processed accurately and on time
• Execute and manage periodic review workflows, coordinating SME assessments and delivering verdicts in compliance with QualiPSO requirements
• Administer workflow management and electronic signature procedures within QualiPSO CMS, ensuring proper routing, review, and approval by authorized personnel
• Maintain and manage the annual Document Plan for GRA, covering new documents, upcoming periodic reviews, planned revisions, and documents scheduled for obsolescence
• Provide expert guidance to ensure key regulatory activities and processes are documented and implemented in compliance with GxP regulations
• Support and advise the Business Process Owner (BPO) network throughout the complete QD lifecycle, acting as a trusted subject matter expert
• Communicate timely updates on new, revised, and obsolete QDs to internal and external GRA stakeholders.

Continuous Improvement Manager

Product Manager

• Oversee the development of product features for decision workflow solutions
• Collaborate with cross-functional teams to define product vision and strategy
• Analyze market trends to inform product development

Digital RnD Decision Fabric – Product Owner

• Applies project management skills and regulatory knowledge for global submission types, from standard to complex
• Applies expert understanding on all dossier formats, standards, navigation and lifecycle management, eCTD, and ICH
• Represents GRO Global Submissions Management on Global Regulatory Teams (GRTs) for assigned development and marketed products portfolio, per the GRA BluePrint model
• Represents GRO Global Submissions Management on Submission Task Force (STF) meetings for major/complex submission filings and partner effectively with regulatory focal points on the Ops-specific details of lifecycle submissions
• Leads discussions with stakeholders and submission task force teams involving electronic guidance issues to ensure an appropriate understanding of electronic submission requirements from a cross-functionally perspective, supporting successful submissions
• Works within project teams in the control of submission component receipt and adherence to submission preparation completion
• Directs the publishing activities for assigned portfolio to ensure high quality and timely submission delivery aligned to both Sanofi and Health Authority standards
• Partners effectively with Submission Leads and global colleagues to deliver high quality and timely Global Simultaneous Submissions (GSS) filing plans, while also providing regional expertise
• Acts as Subject Matter Expert (SME) in audits/inspections, special projects and issue resolution for regional activities
• Partners with GRA and Digital functions as SME for current processes/data/technologies, as well as evaluating and implementing new/emerging technologies and requirements

Global Submission Manager

Business Intelligence Analyst

• Conduct stakeholder interviews, workshops, and requirements gathering sessions to understand business reporting needs.
• Create Reports and Dashboards to support the needs of the PSS Operations Teams.
• Identify trends to gaps and improve productivity/operational efficiencies.
• Assist with data quality checking and clean up.
• Participate in the design, build, and implementation of any/all related CRM initiatives including writing user stories, participating in grooming sessions, sprint planning, and executing UAT scripts.
• Support PSS data management strategy in the design, integration, and migration activities.
• Develop deep knowledge of the patient journey, platforms, and systems used to support our patients and providers.
• Work with our internal and/or external teams to support and or troubleshoot issues as needed.

Real Time Reporting Analyst

• Engage with Hemophilia Chapters and Foundations as a strategic business partner
• Conduct formal and informal presentations to the bleeding disorder community
• Collaborate with field teams to ensure strategic and tactical cohesiveness
• Manage territory Specialty Pharmacy relationships and plan educational programming
• Capture feedback derived from brand needs through interactions with the bleeding disorder community
• Plan and execute Chapter engagements and executive encounters at conferences

Community Relations & Education Manager

Strategy

• Identify opportunities for digital endpoint/outcomes strategies in collaboration with clinical teams to integrate novel and fit for purpose digital measures into clinical studies.
• Work closely with therapeutic area teams to understand strategic needs across Sanofi’s portfolio and establish and understand DHTs available to create value for patients, programs, and operations.
• Lead cross-functional teams in creating integrated plans to develop, validate, and deploy digital endpoints.
• Operationalize digital endpoint strategy programs and serve as the primary point of contact, organizing and managing multi-workstream efforts to meet strategic goals.
• Create and execute integrated validation and testing plans to support strategic study timelines and goals.
• Integrate essential inputs such as health authority feedback, legal, intellectual property, data use, and privacy considerations into the Digital Endpoint strategy to ensure feasibility.
• Represent Sanofi Clinical Innovation internally and externally to the biopharma and digital biomarker communities.
• Contribute to the growth of the digital biomarker organization, identify unmet needs within the organization with respect to process and strategy, propose and execute solutions.

Clinical Strategy Lead – Digital Endpoints

Payroll

• Involved in all aspects of U.S. Payroll tax compliance.
• Assisting in the preparation and timely filing of federal consolidated returns and state/local payroll tax returns.
• Preparation and management of the federal/state tax estimate and extension process.
• Develop responses to state and local tax notices.
• Assist with federal and state tax audits including compiling documentation, reports and/or analytics.
• Researching transaction tax issues, investigating employee tax inquiries and responding appropriately.
• Interpreting and complying with state, local, and international statutes, regulations, and legislation.
• Preparing and/or reviewing indirect tax filings.
• Preparing quarterly tax fillings for Puerto Rico Chauffer’s Tax.
• Tax Quarter Tax Filing Reconciliation in accordance with ADP deadlines.

Payroll Tax Analyst

• Conduct independent review of advertising and promotional materials
• Develop and implement regulatory strategies for promotion and advertising campaigns
• Serve as primary liaison with FDA for assigned products
• Provide guidance and feedback to internal Sanofi constituencies
• Ensure successful implementation of regulatory strategic objectives

Senior Manager, Regulatory Affairs – Advertising and Promotion

Clinical Research

• Act as a mentor for other CRDs and Clinical Scientists on a same project/TA
• Collaborate with functions to ensure uniform, aligned operational approach
• Provide medical expertise to the clinical studies
• Support other clinical development activities
• Contribute to the clinical part of submission dossier for their projects
• Interact with other CRDs in the project, Global Project Head, The PV Rep, Regulatory and other key functional reps

Senior Clinical Research Director, I&I

Director

• Assist the Business Insights & Solutions team with new PBM models
• Ensure holistic view across PBM, Payer, & Employer strategies
• Build disruptive prototype models in collaboration with teams
• Own innovation workstreams with actionable plans
• Develop value-based and risk-sharing models for market access
• Support planning and executing successful new product launches
• Monitor US healthcare environment for trends and changes
• Collaborate with internal stakeholders to identify analysis requirements

Director, PBM Expert, Business Insights and Solutions

Artificial Intelligence

• Own the strategy and vision for PPA and External Data domains
• Lead development of executive-level dashboards leveraging Planisware, Enrich, and Veeva Vault RIM
• Oversee delivery and continuous improvement of PPA systems
• Own the end-to-end lifecycle of external data sharing platforms
• Lead a team of Data and AI Product Owners delivering PPA and external data products

Head of PPA, External Data and AI Workflows

Account Manager

• Educate stakeholders on operational aspects of Tzield administration and integration
• Share insights and best practices from publicly available resources to support infrastructure planning for Tzield
• Develop a deep understanding of each account’s T1D care landscape
• Collaborate with Sanofi teams to create and execute strategic account plans