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Sanofi
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  • Senior Program Manager - Immunology  

    - Cambridge
    Job Title: Senior Program Manager - ImmunologyLocation: Morristown, NJ... Read More
    Job Title: Senior Program Manager - ImmunologyLocation: Morristown, NJ Cambridge, MAAbout the JobJoin 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.The SPM will support the business-related initiatives for his/her respective Therapeutic Area (TA). This individual will work closely with his/her respective Medical Program Lead (MPL) and TA Global Medical Team (GMT), both internally and with our collaborative Alliance partner (when applicable), to support the operational execution of LCM-related initiatives as well as various programs including launch deliverables depending on the LCM of the product. The individual in this role, while working in a matrix team of people and resources, will support the TA-specific Medical Program Lead and GMT to ensure alignment of key activities outlined in the Global Medical Plans.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 ResponsibilitiesProvide Program Management support for his/her respective TA in close partnership with his/her respective MPLPartner with respective Global Medical Director to operationalize Global Medical Team(s)Partner with respective Global Medical Director, Brand team and functional leads in the Global Medical Planning process (Plan generation, tracking and updating)Provide Program Management support relative to LCM management including overall processes, timelines, budget and coordination thereof for the following:Partner with medical team and finance to facilitate financial planning exercises, tracking, and enable execution across Immunology with a heavy emphasis on medical stakeholder transparency.Data Gap / Study prioritization exercisesCSS - approval coordination and central source in Medical for CSO communications and partnershipsPartner with key functional key stakeholders to capture all operational details of ISS, RWE, study data milestones, and budget specific to all studies defined in the Medical planCompliance reporting for CSSOptimize communication and decision-making by ensuring cross-functional representation at relevant team meetings as well as various Medical Affairs’ programs.Support all operational activities to ensure work flow and processes are efficient and compliant with internal SOPs and external guidelines.Manage portfolio & operational level activities via a harmonized Program Management Tool to be used across the SG MPM organizationBuild and maintain strong and collaborative partnerships with internal and external parties. Serve as an advocate for the overall collaboration with our alliance partners (where applicable) and its objectives.Provide Program Management support for various initiatives specific to TAAbout YouRole RequirementsThe ideal candidate will have background in biotech/pharmaceutical industries as well as direct experience in Project/Program Management; scientific background and Medical Affairs experience preferredBachelor of Science (BS) required, advanced degree in science preferred, MBA is a plusAt least 3+ years of project/program management or relevant experience in biotech/pharma or clinical/scientific environmentAbility to lead project and implement strategy into tactical planThorough understanding of project/program management techniques and methodologyAbility to foster teamwork and collaboration coordinating cross-functional teams (matrix environment)Ability to manage projects with minimum supervision from end to endAbility to establish and provide frequent reporting dashboards with key metrics utilizing harmonized methodologies within our organizationStrong interpersonal and communication experience with the ability to effectively interface across all levels of the organization, strong organizational skillsAbility to multitask and maintain tight timelines and priorities in a highly professional mannerExcellent knowledge of MS Office; working knowledge of program/project management softwareCore CompetenciesAct for Change- embrace change and innovation to initiate new and improved ways of working.Cooperate transversally- collaborate effectively with peers, stakeholders and partners across the organization, within and across GBUs, to positively impact business results.Strategic Thinking & Decision Making – ability to think and plan broadly and long-term to inspire excellence in execution and timely decision making based on information available.Location: Headquarters – Cambridge, MAWhy 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.#GD-SG 
    #LI-GZ #LI-Onsite
    #vhdPursue , discover Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.The salary range for this position is:$122,250.00 - $176,583.33All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the . Read Less
  • Clinical Research Director - Oncology  

    - Cambridge
    Job Title: Clinical Research Director - OncologyLocation: Cambridge, M... Read More
    Job Title: Clinical Research Director - OncologyLocation: Cambridge, MA, Morristown, NJAbout the JobJoin 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.As a Senior Clinical Research Director (Senior CRD) within the Oncology Therapeutic Area, you will lead the clinical trial strategy for one or more multiple myeloma assets, creating synergies across Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish the development strategy and execute the development plan.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 ResponsibilitiesWorking within a matrix model, establish or adapt clinical development and contigency plans by engaging with clinical investigators, advisors and regulatory authorities.Author protocols, extended synopses, clinical sections of the Investigator Brochure, IND/IMPD fillings, annual reports, development risk management plans.Lead the clinical interpretation of study resultsContributes to clinical study reports and clinical summaries, including regulatory submissions.Provide expert medical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine, to ensure optimal planning and execution of clinical trialPresent and discuss development strategy and clinical study results with key internal stakeholders, external investigators, advisory boards, and regulatory authorities Author clinical abstracts, presentations for conferences, and manuscripts
    About YouEducationMedical Doctor (MD) or equivalent; training in Oncology and/or Hematology, preferably with experience in myeloma or hematologic malignancies is a plus.ExperienceAt least 4 years experience in clinical development in the pharmaceutical industry, CRO, or healthcare institutionSoft skillsExcellent communication skills (verbal and written English) with both internal and external stakeholdersAdept at problem solvingThoughtful risk-taking: challenge decisions and status quo with a risk-management approachDemonstrated ability to work with a multi-functional team to achieve project milestones.Understanding of and willingness to meet applicable regulatory, quality and compliance standards.Quality-focused, adept at developing good practices, open-minded to data-driven approaches and new digital solutionsInternational/ intercultural working skillsPreferred location is Cambridge, MA. Morristown, NJ and Vitry, France considered.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.#GD-SA
    #LI-SA
    #LI-Onsite
    #vhdPursue , discover Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.The salary range for this position is:$236,250.00 - $393,750.00All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the . Read Less
  • Summer-Fall 2026 Co-Op - Clinical Project Operations  

    - Cambridge
    Job Title: Summer-Fall 2026 Co-Op - Clinical Project OperationsLocatio... Read More
    Job Title: Summer-Fall 2026 Co-Op - Clinical Project OperationsLocation: Cambridge, MAAbout the JobJoin 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 millionsA 4-6 month Co-op/internship opportunity within Sanofi's Clinical Project Operations department, supporting the Clinical Operations Project Lead (COPL) in the Rare Disease therapeutic area. This position offers hands-on experience in clinical operations while providing comprehensive exposure to various aspects of clinical trial design, execution, and modernization strategies.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:Gain comprehensive understanding of clinical operations department structure and functionsSupport study team in development, review, and finalization of study-specific documentsAnalyze phase 2/3 clinical research study design and startup processesResearch and understand disease epidemiology and treatment strategiesUnderstand study site and country selection processes and enrollment strategiesEvaluate changes in global regulatory and healthcare landscapes affecting study design and conductConduct comparative analysis of global regulatory practicesDevelop recommendations for modernizing protocol design to enhance patient enrollment and optimize operational executionPrepare comprehensive documentation of research findings and recommendations, culminating in delivery of a 30-minute presentationAbout YouBasic Qualifications:Currently enrolled and pursuing a master's degree in public health Must beenrolled inan accredited college or university throughout the duration of the co-op/internship.Must be able to relocate to the office location and work 40hrs/week, Monday-Friday, for the full duration of the co-op/internshipMust be permanently authorized to work in the U.S. and not require sponsorship of an employment visa (e.g., H-1B or green card) at the time of application or in the future. Students currently on CPT, OPT, or STEM OPT usually require future sponsorship for long term employment and do not meet the requirements for this program unless eligible for an alternative long-term status that does not require company sponsorshipPreferred Qualifications:Strong analytical and research skillsExcellent written and verbal communication skillsProficiency in Microsoft Office suitePrevious exposure to clinical research or healthcare settingsKnowledge of clinical trial processes and terminologyExperience with data analysis and presentationUnderstanding of regulatory frameworks in healthcareBackground in public health research methodologiesWhy 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.#GD-SA 
    #LI-SA
    #LI-Onsite#vhd Pursue , discover Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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. Read Less
  • Digital Product Owner - NGS & Genomics Platforms  

    - Cambridge
    Position OverviewWe are seeking a Product Owner - NGS & Genomics Platf... Read More
    Position OverviewWe are seeking a Product Owner - NGS & Genomics Platforms to join our In Silico Transversal Data Analytics team within Digital R&D. This role will support the development and implementation of cross-functional in silico capabilities that serve multiple business functions across R&D.As a Product Owner, you will own end-to-end execution of critical platform migrations and capability onboarding initiatives, working closely with the Head of In Silico Data Analytics Products to accelerate our portfolio delivery and enhance user experience across R&D.This is an excellent opportunity for a mid-career product professional with bioinformatics expertise to make a significant impact on Sanofi's digital transformation in drug discovery and translational research.Key ResponsibilitiesProduct Ownership & Execution (60%)Own the planning and execution of analytics platform optimization and migrations.Lead user research, requirements gathering, workflow analysis across R&D functionsCoordinate with technical delivery teams to ensure robust implementation and data integrity and management of use case definitions for SaaS projectsManage day-to-day vendor relationships and operational coordinationUser Adoption & Change Management (30%)Create and execute user adoption strategies for platform transitions through training materials, documentation, and user enablement programsConduct stakeholder interviews, gather feedback for continuous improvementMonitor usage metrics and user satisfaction to measure adoption successIdentify and address barriers to adoption across different business functionsStrategic Support & Collaboration (10%)Support omics strategy development through user discovery, landscape analysisContribute to evaluation of emerging technologies and new capability opportunitiesCollaborate with technical Product Owners and scientific stakeholders across business functions to make strategic platform decisionsABOUT YOURequired QualificationsEducation & ExperienceBachelor's degree in bioinformatics, Computational Biology, Genomics, or related field and 3-5 years experience in bioinformatics, genomics platforms, or computational biology research ORBachelor's degree in business administration, Health Data Science, or Digital Health or related field, and 3-5 years experience in digital transformation or life sciences product management1-3 years specific product management or ownership experience OR experience with data foundations, cloud-based solutions, or data and digital transformationsDemonstrated experience with platform migrations or technology transitionsTechnical ExpertiseHands-on experience with NGS pipelines (bioinformatics, alignment, variant calling, annotation & normalization)Understanding of multi-omics data types (genomics, transcriptomics, proteomics, metabolomics)Experience with Cloud-based genomics analysis platformsProduct Management SkillsStakeholder management across technical, scientific, and digital process teamsPlatform migration or technology transition experienceUser research and requirements gatheringChange management and user adoption strategiesExperience with knowledge management tools (Confluence, Sharepoint)Soft SkillsStrong written and verbal communication with scientific audiencesLeadership and alignment with business process stakeholdersCross-functional collaboration and conflict resolutionTechnical writing and documentationSelf-starter with ability to work independentlyProblem-solving and analytical thinkingPreferred QualificationsMasters/PhD in relevant fieldPrior pharmaceutical or biotech industry experienceExperience with R&D digital transformation in biopharmaExperience with Sanofi platforms or similar enterprise environmentsProject management certification (PMP, Certified Scrum Master)Experience with vendor management and contract coordinationKnowledge of FDA/EMA regulatory requirementsWHAT WE OFFERProfessional GrowthOpportunity to work on high-impact initiatives that directly support drug discovery and patient outcomesExposure to cutting-edge technologies in genomics, multi-omics, AI/ML applicationMentorship from experienced product and scientific leadersClear path for career progression and expanded responsibilitiesAccess to continuous learning and professional development programsImpact & InnovationShape the future of in silico capabilities across Sanofi's R&D organizationWork at the intersection of bioinformatics, product management, and drug discoveryCollaborate with world-class scientists and technical teamsInfluence strategic decisions on technology adoption and platform investmentsWork EnvironmentCollaborative, cross-functional team environmentFlexible work arrangements (hybrid model)Global exposure working with teams across multiple countries and time zonesAccess to state-of-the-art digital tools and platformsCulture of innovation, continuous improvement, and scientific excellenceWhat We're Looking ForWe're seeking candidates who demonstrate:Technical Credibility: Can speak the language of bioinformaticians and understand NGS workflowsExecution Excellence: Record of timely, high quality delivery on complex projectsUser Empathy: Interest in understanding user needs and improving their experienceStrategic Thinking: Ability to connect tactical execution to broader strategic goalsCollaborative Spirit: Work effectively across functions to build strong relationshipsGrowth Mindset: Eager to learn, adapt, and take on increasing responsibilityPursue , discover Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.The salary range for this position is:$108,750.00 - $181,250.00All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the . Read Less
  • Sr Director PSS, HCP Experience  

    - Cambridge
    Job Title: Sr Director PSS, HCP ExperienceLocation: Cambridge, MA, Mor... Read More
    Job Title: Sr Director PSS, HCP ExperienceLocation: Cambridge, MA, Morristown, NJAbout the JobJoin 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.At Sanofi, we are dedicated to transforming patient health through chasing the miracle of science. As a prominent pharmaceutical manufacturer, our commitment extends beyond drug development, ensuring that patients can access and afford our therapies.The Sanofi Patient Support Services (PSS) team is focused on supporting patients wishing to access Sanofi therapies. This is achieved by offering programs that provide reimbursement and logistics support, financial assistance, and patient education. In addition to the program offerings, the PSS organization is also home to field teams that provide education and support to patients and customers.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:Enterprise Strategic Leadership RoleAs a pivotal member of Sanofi's PSS Evolution & Strategy leadership team, the Senior Director of HCP Experience Strategy will architect and drive enterprise-wide transformation of our Patient Support Services (PSS) from the perspective of the HCP experience. This strategic enterprise position leads large complex initiatives, directs organizational strategy, and drives measurable business outcomes that advance Sanofi's market leadership in Patient Support Services.Strategic Leadership & Enterprise ImpactDrive enterprise-wide strategic vision and multi-year transformational initiatives across Sanofi's specialty care portfolioStrategically align and mobilize your team as well as cross-functional partners towards enterprise objectives, ensuring resources are optimized to drive maximum business impact and organizational effectivenessPartner with PSS senior leadership to shape strategy and implementation planningEstablish thought leadership in patient access innovation, setting industry benchmarks and standardsChampion data-driven frameworks that guide enterprise-level decision makingDevelop solutions to complex healthcare access challenges through forward- thinking strategies and innovationPeople & Team LeadershipBuild, develop and lead a high-performing team of strategists focused on evolving and building a future ready HCP PSS ecosystemDrive talent acquisition, development, and succession planning.Foster a culture of innovation, accountability and measurable business impactLead direct reports and cross-functional matrix teams through strategic alignment, design and build phases for large strategic initiativesOwn multi-year strategic planning with direct accountability for business outcomesEstablish enterprise-level KPIs and performance metrics that drive business growth and oversee large enterprise vendor managementArchitect comprehensive strategic roadmaps guiding PSS evolution of the HCP experience.Cross-Functional Leadership & InfluenceLead enterprise-wide transformation initiatives impacting multiple therapeutic areasBuild strategic partnerships with key stakeholders across Specialty Care and General Medicine business unitsDrive organizational change management and adoption at scaleAbout YouRequired QualificationsBachelor's degree in Business, Life Sciences, or related field10-12+ years progressive leadership experience in pharmaceutical / healthcare industry with at least 5+ in Patient Support ServicesDemonstrated experience managing multi-million-dollar budgetsDeep understanding of PSS landscape, including hub services, patient access, and healthcare provider needsProven ability to lead both directly and indirectlyDemonstrated ability to lead cross-functional teams through multiple large complex projects simultaneously.Preferred QualificationsAdvanced degree preferred (MBA, PharmD)Proven executive presence with track record of ability to influenceTrack record of driving enterprise-wide transformation with measurable business impactExcellent communication and collaboration skills, with the ability to influence and work effectively across all levels of the organization.Ability to think strategically and translate vision into actionable plans.This leadership position represents a unique opportunity to drive enterprise transformation and shape the future of Patient Support Services at Sanofi. The role demands visionary leadership, business acumen, and the ability to deliver measurable impact at scale in support of our mission to improve people's lives through the miracles of science.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.#GD-SG 
    #LI-GZ #LI-Onsite
    #vhdPursue , discover Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.The salary range for this position is:$202,500.00 - $292,500.00All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the . Read Less
  • Medical Science Liaison - Gastroenterology - Chicago  

    - Cambridge
    Job Title: Medical Science Liaison - Gastroenterology - ChicagoLocatio... Read More
    Job Title: Medical Science Liaison - Gastroenterology - ChicagoLocation: Remote/Field, Illinois, Iowa, Minnesota, Missouri, Wisconsin regionAbout the JobJoin 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.The Medical Science Liaison (MSL) is field-facing role whose main objectives are to:Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products.Execute on stakeholder engagement plans to gather data, develop and share medical insights that contribute to enhancement of Sanofi’s key medical messages, plans and future research.Keep abreast of medical and scientific developments in the therapeutic field to help identify and critically assess research opportunities and to play a supportive role in the execution of evidence generation plans to enhance the value of our products in a real-world settingRecognize, record and share insights that deepen our understanding of the needs of patients, consumers, regulators, payers, and healthcare providers and proactively contributes towards identifying unmet needs.Maintain effective and appropriate communication among internal stakeholders (Medical Affairs colleagues, Medical Information and Commercial Operations) while maintaining full compliance with relevant company, industry, legal and regulatory requirementsDemonstrate operational understanding and risk management by ensuring excellence in execution of all governance processes.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:Engages external stakeholders on medical and scientific information exchange for the therapeutic area during an one-on-one interactions and group settings, exhibiting excellent scientific and clinical knowledgeUses strong knowledge of relevant diseases and disease management protocols, healthcare environment and competitors to articulate the medical and scientific value of our products with external experts.Establishes robust, long-term peer relationships with Key Opinion Leaders and other stakeholder partnersActively engages with appropriate stakeholders on medical, clinical, epidemiologic, and scientific topics to advance their understanding of the disease by sharing information and answering questions based on approved material within Regulatory guidelines.Engages with appropriate stakeholders to understand the state of healthcare policies and guidelines as they relate to clinical practices at a local, state, regional, federal, or national level.Uses defined systems to maps, identify, profile, and prioritizes stakeholders in line with the therapeutic area medical plan and looks for opportunities to collaborate and build a value based partnership addressing the HCPs therapeutic goals.Effectively utilizes the Scientific Engagement Model to plan territory and individual stakeholder (Key Opinion Leaders, payers, HCP etc.) medical strategy and engagement interaction plans consistent with the Field Base Medical Activity Plan and medical function priorities.Effectively utilizes the Scientific Engagement Model for attending and establishing a Sanofi Medical presence at relevant scientific congresses, symposia as directed.Organizes educational meetings or local scientific advisory boards when requested.Support speakers training to ensure continued scientific support in the field.Responds to unsolicited request for medical information associated with supported products and disease state area.Gathers data and generates insights from stakeholder interactions and provides feedback to the organizationRecognize and collect feedback/reactions from multiple data sources and various stakeholders.Record/report insights and information appropriately, using available mechanisms and tools.Critically and routinely evaluate and discern from the information gained from published studies, and stakeholder interactions to develop key insights that deepen our understanding of the market’s needs and opinions of external stakeholders and therefore contribute to enhancement of Sanofi’s scientific messages, plans, strategy, systems, and product development.Maintain awareness of and assesses emerging evidence in disease area to educate and enhance discussions with key stakeholders.Collaborates effectively with internal stakeholdersDistribute relevant scientific and medical information and key external insights to internal stakeholders when requested.Collaborate, as directed, with Commercial Operations, Business Development, Regulatory, etc. to facilitate diligence reviews, medical and safety evaluation, product positioning, lifecycle evidence planning, and compliance needs.Contribute to the creation of material for internal and external stakeholders where applicable, following internal Sanofi policies, and Federal and National Policies as applicable.Supports evidence-generation activities by aiding in data acquisition and identifying opportunities for further data collection clinical or investigator-ledMonitors disease epidemiology and provides support, including protocol development, when needed on various types of studies: long-term surveillance, compliance, pharmacovigilance, and effectiveness studiesIdentifies data collection opportunities during stakeholder interactions and reports these using approved processes.Maintains awareness of clinical trial activity within territory and suggests clinical trials sites as requested.Responds to unsolicited requests regarding interest in investigator sponsored studies (ISS), and supports ISS submissions through appropriate internal processesContext of the job/major challengesAble to operate independently (with minimal supervision) and navigate complex regulatory environments in person and via digital channels from remote (non-office based) environment.Possible substantial travel: nationally and internationally.Effectively mediate KOL's complex and controversial opinions vs; corporate policy decisions ensuring KOL relationships/medical strategy are not negatively impacted.Ensures regulatory boundaries re non-promotional activities are respected vis-à-vis commercial partners.Scope of Role / OutputsManage a base of 50 stakeholders; developing and maintaining stakeholder engagement tracking database.Territory covers Illinois, Iowa, Minnesota, Missouri, Wisconsin regionPlan day-to-day interactions, including discussion points in accordance with Medical Affairs strategy, establishing a frequency of interactions per stakeholder per year to ensure that objectives are met.Accountability for US KOLs with reporting mainly to Medical AffairsExecutes on defined KOL territory strategy that is targeted to address diverse stakeholder needs (payers, patients, KOLs, HCP etc.) and is aligned with company objectives.Develops relevant territory engagement plans in line with the medical strategy and supports the team’s medical plan execution.Uses approved scientific data during KOL interactions to advance the understanding of the therapeutic area.About YouQualificationsAdvanced degree in a technical, scientific or medical field (MD, PhD, Pharm D,) preferred, or other Relevant Life Science degree (RN/MS) with Rhinology and/or Gastroenterology Specialty required.Must reside in territory.Valid driver’s license with a clean driving record and ability to pass a complete background check.Driving a company car in a safe manner to daily meetings and appointments is required.Responsible for operating the motor vehicle using safe driving practices, knowledge of and compliance with all company policies, and obeying all traffic laws.ExperienceMinimum of 2 years of experience in pharmaceutical industry, Medical Science Liaison role, or relevant clinical practice. Additional years of experience are an asset. MSL experience strongly preferred.Candidates with relevant Immunology clinical experience consisting of Gastroenterology clinical environment may be considered.Clear understanding of medical practice, clinical decision making, and healthcare systems related to patient care.Ability to interpret key scientific data and translate this information to meet educational and research needs.Demonstrated ability to address educational and research needs through delivery of cutting edge scientific/evidenced based data.Understand the design and execution of research studies.Exemplary communication and presentation skills.Experience in working on multi-disciplinary teams and managing significant volume of projects.Candidates with relevant Immunology clinical experience consisting of Gastroenterology clinical environment may be considered.Skills/KnowledgeActively listens to others and is adept at confidently stating expert opinion while respecting the positions of others - can exert diplomacy while standing firm on a position.Utilizes effective, professional communications to cultivate strong working relationships with internal and external colleagues, flexible in own approach to people and situations.Skillfully plans, prioritizes, and executes multiple responsibilities and projects.Demonstrates effective leadership skills (by example and through accomplishments), steps forward to handle challenges within scope of authority.Deep understanding and knowledge of local regulations and codes of practice for pharmaceutical industry, in particular as they apply to the non-promotional activities of this role.Demonstrates scientific expertise - stays abreast of data, treatment trends, and new information in the profession and ability to articulate therapeutic knowledge and translate expert feedback into appropriate insights.Knowledge of relevant healthcare systems, the evolving medical landscape, regulatory and payer environment, public health and industry trends.Proficiency in digital tools.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.This position is eligible for a company car through the Company’s FLEET program.Candidates must complete all fleet safety training and must maintain an acceptable driving record regarding accidents and incidents.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-Remote
    #vhdPursue , discover Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.The salary range for this position is:$144,750.00 - $209,083.33All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the . Read Less
  • Head of U.S. Health Economics & Value Assessment (HEVA)  

    - Cambridge
    Job Title: Head of U.S. Health Economics & Value Assessment (HEVA) Loc... Read More
    Job Title: Head of U.S. Health Economics & Value Assessment (HEVA) Location: Cambridge, MA, Morristown, NJAbout the JobJoin 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.The Head of U.S. Health Economics & Value Assessment (HEVA) is a senior strategic and scientific leader responsible for shaping and executing the U.S. HEVA strategy for Sanofi’s Specialty Care portfolio, the company’s largest and most complex market and region.Reporting to the GlobalHead of HEVA, Specialty Care, with a dotted-line accountability to the U.S. Specialty Care Business (Value & Access or U.S. Head), this role leads a team of U.S. HEVA Therapeutic Area (TA) Leads who deliver the evidence and insights needed to ensure access, inform policy, and demonstrate value throughout the product lifecycle (from launch through post-launch optimization).The U.S. HEVA Head is a strategic business partner and thought leader—translating global evidence into US regional impact, delivering US specific evidence generation and dissemination, shaping payer and policymaker dialogue, and ensuring HEVA evidence directly influence pricing, access, and policy decisions. This is a market-facing, enterprise-critical leadership role that ensures Sanofi’s evidence translates into real-world impact in its most commercially significant region.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:Strategic Leadership and Market ImpactDefine and execute the U.S. HEVA strategy across all Specialty Care therapeutic areas, aligned with global HEOR, U.S. Medical, and Commercial priorities.Serve as a member of both the Global HEOR Leadership Team and the U.S. Specialty Care Leadership Team, ensuring full alignment and integration between global and US regional strategies.Translate HEVA evidence into business and policy impact—driving payer engagement, value positioning, and access strategies.Anticipate and proactively address U.S. policy and reimbursement dynamics (eg, PDAB, ICER, IRS, MFN) through strategic evidence planning and engagement.Represent Sanofi externally as a U.S. HEVA thought leader, advancing the role of evidence in access, policy, and clinical decision-making.Evidence Generation and DisseminationOversee design and execution of U.S.-focused HEVA inclusive of RWE program that demonstrate product value across diverse payer and healthcare systems.Lead launch excellence and post-launch US specific HEVA strategies, ensuring evidence generation aligns with U.S. access, pricing, and policy needs.Develop and guide compliant and impactful US evidence dissemination pathways (eg, HCEI, PIE, CFL, etc.)—including publications, payer dossiers, field materials, and digital platforms.Partner with U.S. Medical Affairs/Value & Access to ensure appropriate use of HEOR evidence in field communications and training.Champion data-driven storytelling that enhances HEVA’s impact and visibility in internal and external forums.Policy, Payer, and Stakeholder EngagementCollaborate with Value & Access, US Medical Affairs, and Policy teams to deliver evidence that informs value frameworks, PDAB and ICER responses, value-based contracting strategies, etc.Partner with State Government Affairs and external advocacy organizations to shape emerging access and affordability policies.Lead engagement with key US policy stakeholders (eg, ICER) to represent Sanofi’s HEVA perspectives and scientific rigor.Support Sanofi’s external advocacy, guidelines, and evidence education initiatives to shape practice and reimbursement in the US.People, Culture, and Organizational LeadershipLead and develop a high-performing U.S. HEVA team, fostering scientific excellence, collaboration, and accountability.Empower U.S. TA Leads to act as strategic partners to the business and thought leaders in their therapeutic areas.Promote a culture of innovation, inclusion, and continuous learning aligned with HEVA's goals.Model integrity, transparency, and ethical leadership in all scientific and operational activities.Performance, Integration, and GovernanceEstablish and track US HEVA performance metrics that demonstrate measurable business impact.Ensure alignment between U.S. and global HEVA priorities, creating a two-way bridge for knowledge sharing, effective hand-off peri-launch and best practices.Oversee budgeting, resourcing, and operational excellence to ensure effective and compliant delivery for the US business.Maintain full compliance with enterprise, legal, and regulatory standards in evidence generation and dissemination specific to the US.About YouEducation:Advanced degree (PhD, MD, MSc, MPH, or PharmD) in a scientific disciplineExperience:Minimum of 10 years of progressive experience in health economics and outcomes research (HEOR), real world evidence, or related evidence and policy leadership rolesProven success leading U.S. HEOR strategy and execution across multiple therapeutic areas within large, matrixed organizationsRecognized externally as a HEOR leader with credibility among payers, policymakers, and academic peersDeep understanding of the U.S. healthcare ecosystem, payer and policy landscape, and evolving regulatory environmentDemonstrated ability to translate evidence into business impact, influence policy, and drive access outcomesExperience managing scientific teams and cross-functional stakeholders at senior enterprise levelsApproximately 25% travel expected, primarily domestic with occasional international trips.Leadership competencies:Strong leadership across strategic, operational, and people dimensions with a track record of team developmentExcellent communication and influencing skills, including the ability to convey complex evidence to senior management and external stakeholdersDeep understanding of the U.S. healthcare, policy, and regulatory environment with a commitment to compliance and ethicsEntrepreneurial and team spirit and ability to develop creative solutions to complex problemsWhy Choose UsBring 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 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.#GD-SG 
    #LI-GZ #LI-Hybrid
    #vhdPursue , discover Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.The salary range for this position is:$258,750.00 - $373,750.00All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the . Read Less
  • Job Title: Governance & Strategic Alliances Lead (EBI NA & Global Spe... Read More
    Job Title: Governance & Strategic Alliances Lead (EBI NA & Global Specialty Care)Location: Morristown, NJ Cambridge, MAAbout the JobReady to push the limits of what’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. We are seeking an experienced compliance professional to lead strategic healthcare compliance initiatives as a key member of the North America & Global Specialty Care EBI (“Ethics & Business Integrity”) team. This Sr Director-level leader will be responsible for enhancing our compliance governance framework, driving strategic healthcare compliance initiatives, partnering with key stakeholders (e.g. internal audit, advisory, legal, privacy, digital), and providing critical compliance oversight for M&A activity and strategic transactions. This role combines tactical leadership with hands-on compliance expertise to ensure integrity across partnerships and operations.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, implement and oversee governance frameworks within the functionPartner with senior leadership to integrate compliance strategies into business objectivesDrive continuous improvement of compliance programs based on industry trends and regulatory changes; design, develop, and implement measures for assessing program effectivenessAdvance, implement, and monitor robust risk mitigation plans and corrective action strategies in collaboration with cross-functional partnersLead EBI/corporate compliance due diligence activities for strategic alliances, partnerships, and key business initiativesPrepare and present comprehensive reports on compliance program activities, risks, and strategic initiatives to senior leadership and Compliance CommitteesManage and coordinate LRIG (Local Responsible Innovation Governance for AI-related initiatives) for North America EBIAssist with third-party risk management and compliance assessment processesAbout YouRequired Qualifications:12+ years of healthcare compliance experience, with 5+ years in leadership rolesDeep knowledge of US healthcare laws, regulations, and industry codesExperience with leading or managing compliance program governance and implementationPrior experience in compliance risk assessment and due diligence processesStrong track record of managing strategic partnerships and alliance relationshipsDemonstrated success with digital tools commonly utilized in healthcare complianceWorking knowledge of AI and desire to implement AI in compliance operationsPreferred Qualifications:JD, MBA, CPA, or advanced degree in related fieldHealthcare/pharmaceutical industry experienceCertification in Healthcare Compliance (CHC) or related credentialsExperience with business assessments and audit processesBackground in managing global compliance initiativesLeadership Competencies:Strategic thinking and business acumenStrong analytical and risk assessment capabilitiesExcellence in stakeholder management and communicationAbility to influence and drive change across organizational levelsFlexibility, tactical decision-making, collaborative mindsetWillingness to embrace new digital tools and related processesWhy 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.#GD-SA 
    #LI-SA
    #LI-Onsite#vhd Pursue , discover Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.Watch our and check out our Diversity Equity and Inclusion actions at !Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.The salary range for this position is:$180,000.00 - $300,000.00All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the . Read Less

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany