Sanofi

Research Analyst

• Orchestrate a highly relevant and impactful insight agenda for the US Systemic Mastocytosis business
• Be a highly valued strategic thought partner to the US Commercial team
• Effectively support / inform standard US Commercial business processes
• Cultivate strong partnerships across a matrixed internal environment
• Cultivate relationships with the Insights vendor community
• Effectively manage projects, driving collaboration between internal and external teams
• Communicate data / insights clearly and concisely

Associate Director, Market Research – Systemic Mastocytosis

Director

• Collaborate with Commercial team, Finance, and other cross-functional partners to develop, document, and communicate accurate patient / volume / revenue forecasts for annual long-term Strategic Planning & Budget cycles, bi-annual medium-term forecast updates, and monthly near-term Rolling Forecast updates.
• Coordinate with Finance business partners and forecasters in other therapeutic areas to coordinate forecast cycle deliverables and promote harmonization across assets & functions.
• In partnership with Analytics & Finance colleagues, provide key end-of-month closing deliverables (i.e., price / volume & demand / inventory analyses).
• Provide monthly updates to Commercial leadership on performance and near-term forecast outlook, integrating latest actuals, analytics, Market Research, CI, etc.
• Support model enhancements to ensure forecasts for in-line & launch products reflect strategic direction of each brand (e.g., segmentation, patient flow, etc.).
• Collaborate with Market Research to plan & design studies that provide key forecast inputs (e.g., demand study / conjoint exercises).
• Partner with Finance and Market Access to incorporate latest GTN and access assumptions, conduct payer mix analyses, and generate price / volume waterfalls.
• Leverage resources such as analogue analyses & external forecasts (e.g., syndicated / analyst reports) to pressure-test and refine forecast assumptions.
• Work with Global forecasting to ensure that US forecast deliverables align to Global guidance and properly integrate with Global forecast aggregation process.
• Work with Finance and Demand Planning to ensure the most appropriate forecast (by SKU) is delivered for monthly supply chain planning activities.
• Collaborate with Marketing, Sales, Patient Support Services and Finance to assess the value of proposed initiatives and / or risks posed by market events; deliver ad-hoc analyses that leverage forecast models to answer key business questions.
• Collaborate with Data Management, Analytics, and external data providers to conduct periodic reviews of key model inputs to ensure forecast accuracy.
• Coach junior team members for onboarding, upskilling and Sanofi specific processes / data.

Associate Director, Forecasting – Systemic Mastocytosis

General

• Provide PV and risk management expertise to internal and external customers
• Maintain knowledge of product, product environment, and recent literature
• Lead cross functional Safety Management Teams (SMTs) and GPE internal Safety Analysis Teams (SATs)
• Communicate with and represent PV position within project/product teams
• Responsible for signal detection and analysis
• Collaborate with Center of Excellence for Signal Detection and Safety Epidemiology group
• Identify and implement proactive safety analysis strategies
• Provide proactive risk assessment
• Represent safety position in cross functional submission teams
• Document, coordinate, review and validate Periodic reports

Global Safety Officer

Medical Director

• 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

Clinical Research Director

QA Engineer

• Ensure implementation and follow-up of actions defined within their area of responsibility.
• Conduct regular Gemba rounds and participate in the self-inspection program.
• Prepare batch records for manufacturing, packaging, and label printing.
• Perform quality review of manufactured or packaged batch records.
• Manage ongoing deviations.

QA Specialist

Data Scientist

• Lead structured data operations end-to-end, ensuring timely and compliant submissions to Health Authorities worldwide.
• Manage and develop a team of structured data specialists to meet all compliance requirements and quality standards.
• Drive the global implementation of IDMP standards and monitor changes to regulatory data requirements.
• Represent Sanofi in working groups with Health Authorities and industry partners to shape regulatory innovation.
• Oversee data quality control and track Key Performance Indicators (KPIs) to ensure on-time submissions.
• Set up and monitor service agreements with vendors and contractors to ensure operational excellence and timely delivery.
• Provide expertise during audits and support inspection processes with required documentation and responses.
• Work with stakeholders to continuously improve structured data processes and build team expertise.

Submission Lead – Structured Data

Medical writer

• Is in charge of creating, writing, and coordinating concept documents, protocols, informed consent forms, and clinical study reports according to Sanofi Pasteur document standards, tools, and SOPs.
• Is in charge of creating, coordinating, compiling, and editing investigator brochures, updated licensure and renewal documents (clinical overviews, addendum to clinical overviews, CTD updates) according to Sanofi Pasteur standards, tools, and SOPs.
• Is in charge of creating, writing, and coordinating CTD clinical summaries and overviews in line with Sanofi Pasteur document standards, coordinating the medical writing CTD activities (interaction with RA and other functions involved), and providing the CTD supportive activities within the medical writing department.
• Participates as a member of the clinical team accountable to the Clinical Team Leader for all project issues (role of referent medical writer).
• Is involved in the peer-review and QC cross-check of documents produced by the Medical Writing platform and in the review of documents produced by other departments (such as SAP and CRF).
• Contributes to the development of document templates and relevant SOPs.
• Represents the platform on committees and working groups within Clinical as requested.
• Provides mentoring support to less experienced colleagues and new Company staff members if needed.
• Provides project management of medical writing deliverables for a trial or project, including negotiating timelines, and identifying and escalating issues to both the clinical team and the local Head of Medical Writing.
• Is in charge of supervising subcontracted medical writing activities if needed. May contribute to the updates of templates, SOPs, and other guides for Medical Writing.

Senior Medical Writer – Vaccine

• Define and own the Health Ecosystem & Innovation roadmap, bringing "outside-in" innovation from start-ups, academia, digital health, and patient communities into Sanofi's medical innovation pipeline.
• Build and manage a strategic external innovation ecosystem encompassing start-up partnerships, academic collaborations, Digital Therapeutics (DTx) alliances, and patient-centric data platforms.
• Lead the Patient centric strategy, building capabilities that improve Sanofi's ability to identify, understand, and engage patient communities in support of medical and evidence-generation objectives.
• Identify, evaluate, and broker partnerships with digital health start-ups and DTx companies whose capabilities complement or enhance Sanofi's medical portfolio and patient engagement strategy.
• Build and maintain a dynamic map of the external health innovation landscape, including competitive intelligence across digital health, AI-powered medical tools, and DTx.
• Represent Sanofi at external innovation forums, accelerators, and academic conferences, serving as the company's ambassador to the health innovation ecosystem.
• Function as the primary incubator for external medical innovation partnerships — manage the full pipeline from opportunity scouting through due diligence, KPI definition, and handoff to GBU operational teams.
• Collaborate with the Global Head of Medical Innovation, GBU leadership, and Digital Partners to assess and prioritize external innovation opportunities based on medical value, technical feasibility, and strategic fit.

Global Lead, Health Ecosystem – Innovation

Strategy

• Deliver CX strategy across digital products and end-to-end journeys for the organization: define plans, principles, based on research and insights and measurement frameworks.
• Ensure CX Strategy meets agreed upon milestones, mitigating risk and maximizing process efficiency.
• Work closely with direct and indirect team members to define, document, share and maintain user experience strategy, rollout, and operations.
• Mentor, share and empower the team to stay informed of changes in the industry.
• Influence product and service strategy direction.

Consumer Experience Strategy Lead

• Lead strategy, roadmap, and lifecycle management of commercial reporting and analytics solutions (e.g., Tableau, Power BI and other enterprise tools)
• Ensure structured reporting is the governed foundation for commercial decision-making, aligned to standardized KPIs, business definitions, and reporting logic.
• Implement and govern AI powered conversational analytics capabilities by ensuring outputs are grounded in trusted reporting frameworks and trusted data sources.
• Partner with Digital and Data teams to integrate AI tools and automation into the reporting ecosystem in a controlled and scalable manner
• Identify opportunities to improve reporting efficiency, insight generation, and user experience through automation and digital innovation to enhance productivity while maintaining explainability.
• Serve as business owner for KPI definitions, semantic alignment, and reporting logic across commercial analytics platforms
• Ensure consistency of business definitions across structured reporting and AI-enabled consumption layers
• Act as key business context expert to ensure AI-generated insights are accurate, explainable, and commercially relevant
• Partner with Data Engineering and Digital teams to ensure semantic models are reflected accurately across reporting and AI tools
• Establish and enforce governance standards for reporting consistency, data integrity, and metric alignment
• Define and manage operating model for commercial reporting, including intake, prioritization, and governance processes
• Direct executional activities (development, QA, maintenance, and operational support) and ensure accountability of hub teams
• Drive scalable, standardized ways of working across distributed teams to improve efficiency and quality
• Implement AI-powered workflows for routine reporting tasks, freeing capacity for higher-value strategic work.
• Serve as strategic partner to Field Leadership, Brand Teams, and Commercial Operations on reporting, analytics, and AI-enabled insights
• Lead communication of reporting changes, ensuring clarity, alignment, and stakeholder adoption
• Enable adoption and effective use of structured reporting and AI-enabled tools through training, guidance, and engagement
• Support change management efforts associated with analytics modernization and AI adoption
• Translate complex commercial data into clear, actionable insights for field and business decision-making
• Implement and scale self-service analytics and AI-enabled exploration capabilities
• Ensure AI-generated insights are validated against governed reporting sources for accuracy and trust.

Associate Director, Field Reporting & Intelligence

• Ensure and develop robust, compliant, and controlled processes for Periodic Safety Report (PSR) authoring and vendor oversight while upholding regulatory compliance expectation
• Lead the Periodic Report Expert (PRE) Team through coaching, mentorship, and development planning according to individual and organizational priorities
• Develop and execute outsourcing strategies for PSR authoring according to business criticality and resourcing needs
• Establish and maintain the annual worldwide regulatory planning of PSRs for the entire company portfolio (clinical and postmarketing)
• Manage PSR Planning Team with regard to PSR planning activities, resource allocation, and training needs
• Serve as system owner for the PSUR Web page Repository and tracking tool database
• Identify, implement, and support process improvements to leverage efficiencies and drive continuous improvement

Global Periodic Reporting Lead

• Reporting into a US Oncology Divisional General Manager, Commercial, assume the commercial leadership role for assigned key accounts
• Develop and execute account plans, providing overall account leadership
• Coach cross-functional team members
• Build a strategic account plan for assigned accounts
• Organize and deploy appropriate resources within SANOFI to drive value co-creation with customers and meet/exceed revenue targets
• Identify and qualify opportunities within accounts and develop growth strategies
• Lead strategy sessions with account teams to facilitate customer value co-creation
• Lead a team of Area Business Managers, ensuring strong field execution and ongoing professional development
• Ensure ongoing compliance and accountability for business outcomes
• Manage regional expenses within allocated budgets

Regional Business Director

Manager

• Partner with the Device Regulatory Lead on assigned projects
• Provide regulatory guidance and advice to Global Regulatory Team (GRT) and cross-functional teams
• Contribute to and execute innovative and sustainable medical device regulatory strategies covering stand-alone medical devices and device part of combination products elements
• Contribute to device Health Authority interactions plan, support device related and cross-functional health authority interactions
• Identifies medical devices regulatory acceleration opportunities and regulatory risks, and proposes thoughtful risk mitigations in collaboration with the GRT
• Identify issues and opportunities that impact submissions timelines; ensures appropriate communication, resolution and/or escalation as needed
• Support global filing and lifecycle management activities for device submissions/device aspects of medicinal product submissions
• Liaises with device, clinical, manufacturing, commercial, and other internal business partners to enable successful regulatory outcomes
• Prepare and review design control deliverables
• Contribute to product development and lifecycle management planning
• Provide regulatory impact assessments for proposed product changes
• Supports operational and compliance activities for assigned deliverables, develops, executes regulatory submission planning activities, including generating submission content plans, submission tracking, communication and document management.

Senior Manager, GRA Device Associate – Medical Devices and Combination Products

• Provide leadership and guidance as the lead statistician on one or more project team(s)
• Act as statistical consultant within company
• Lead one moderate project, one or several indications, or a highly complex large study (eg. CVOT) in late phase or Onco early development and lead multiple projects
• Direct statistical support and provide scientific leadership for responsible projects
• Accountable for statistical aspects of early or late clinical development/medical affairs plans, studies, and submissions activities
• Mentor people working on the project
• Promote teamwork, quality, operational efficiency, and innovation
• Ensure project team compliance with SOPs and departmental standards

Statistical Project Leader

Clinical Research

• Support the design and execution of multiple clinical studies across the development plan
• Help prepare key trial documents — protocols, informed consent forms, and benefit-risk assessments
• Contribute to CRF design and review completion instructions
• Support study start-up, site opening, and enrollment monitoring
• Review and analyze data listings, patient profiles, and key study data within statistical reports
• Partner with Data Management to generate relevant queries
• Stay current on competitive data and the therapeutic landscape
• Deliver clinical landscape and benchmark updates to the CRD and Project Lead
• Partner with Clinical Leads and CRDs to build presentations for governance committees
• Serve as delegate for the CRD in developing and overseeing the clinical development plan
• Act as liaison across data management, biostatistics, medical writing, pharmacovigilance, regulatory affairs, clinical operations, and translational medicine
• Support project team members, project management, and medical affairs
• Co-author briefing packages for health authority submissions and contribute to regulatory strategy
• Build and maintain relationships with internal collaborators, KOLs, and investigators
• Support interactions with Sanofi governance bodies, external partners, and committees