Urwah Admin

Sanofi

<div>Job title: Team Lead, Supply Chain for External Manufacturing Management<ul><li> 
Hiring Manager: Head of M&amp;S Services Hyderabad</li><li>
Location: Hyderabad</li></ul><ul><li> % of travel expected: As per business need</li><li> Job type: Permanent</li></ul> 
About the job
This leadership position drives strategic supply chain operations for external manufacturing network, providing comprehensive oversight of Contract Manufacturing Organizations and business partners while ensuring optimal supply chain performance. The Lead develops and implements supply chain strategies, manages complex stakeholder relationships, and drives continuous improvement initiatives to deliver products meeting Quality and Regulatory standards while optimizing costs, timelines, and service levels. 
Our Team:
Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions. 
As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability &amp; interoperability and thus accelerate impact on global health. 
The Global M&amp;S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting Global M&amp;S teams by acting as a crucial link between our R&amp;D and Manufacturing facilities, playing a vital role in securing the present portfolio and delivering future launches of high-quality and innovative drugs and vaccines. 
Main responsibilities:<ul><li>
Strategic Demand &amp; Supply Management: Lead forecast analysis and production planning strategies, oversee order management from launch to delivery optimizing efficiency and costs, lead complex packaging item change initiatives across CMO and markets, optimize supply chain inventory strategies and record management.</li><li>
Strategic Relationship &amp; Crisis Management: Lead relationship management with CMO driving feasibility improvements and stock optimization strategies, establish crisis management protocols and communication frameworks for restrictive environments, oversee supply chain performance including yield optimization and obsolescence reduction, drive reporting excellence and crisis resolution strategies, lead cross-functional collaboration with Quality and Regulatory departments ensuring impact assessment and mitigation.</li><li>
Advanced Toll &amp; Sourcing Management: Lead API forecast analysis and strategic planning, oversee complex order management and delivery optimization to CMOs, establish API level strategies at CMO sites ensuring production continuity and optimal stock policies, lead reconciliation processes and stock adjustment protocols between Sanofi and CMO inventories, drive double sourcing strategies and alternative source development initiatives.</li><li>
Performance Leadership &amp; Innovation: Lead monitoring and optimization of group supply indicators (out-of-stock rate, supply alerts, customer service level, inventory level, stock policy), drive cross-functional improvement initiatives and strategic business projects, lead serialization and track &amp; trace implementation strategies, coordinate complex divestment and pruning initiatives.</li><li>
Strategic Budget &amp; Business Development: Lead budget development and volume trend analysis, drive portfolio cost optimization strategies, implement cost-effective supply chain process innovations, ensure compliance with evolving legal requirements and standards, lead cross-departmental collaboration for strategic business growth planning, mentor team members and drive supply chain excellence culture.</li></ul> 
About you<ul><li>
Experience: 8-10 years recognized experience in supply chain, planning, and demand management with proven leadership track record, and extensive pharmaceutical industry experience preferred</li><li>
Soft skills: Strong leadership and team development capabilities, (direct management) high autonomy and strategic thinking, excellent reactivity and anticipation skills, advanced teamwork and networking abilities, strong negotiation and influencing skills, entrepreneurial initiative, results and performance-driven mindset</li><li>
Technical skills: Expert knowledge of SAP and supply chain systems (Kinaxis), deep pharmaceutical industry expertise, advanced project management in complex environments, supply chain strategy and optimization, digital transformation capabilities</li><li>
Education: Master&rsquo;s degree in supply chain, Engineering, Business, or related field, additional leadership or business qualifications preferred</li><li>
Languages: Fluent professional English (written and spoken)</li></ul> 
Pursue progress, discover extraordinary 
Better is out there. Better medications, better outcomes, better science. But progress doesn&rsquo;t happen without people &ndash; people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let&rsquo;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, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! 
This job post is subject to local legal and social procedures where applicable.
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Team Lead, Supply Chain for External Manufacturing Management

<div>Mission statements<ul><li>
The Statistical Programmer will work with Medical Affairs biostatisticians and MedHub biostatistics and programming personnel to implement statistical analysis plans and provide QC&rsquo;d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, and manuscripts)</li><li>
The Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques</li><li>
The Statistical Programmer will ensure SOPs are followed and timelines and quality are met</li></ul>
Collaboration<ul><li>
Local biostatistics and programming teams</li><li>
Global Medical Affairs biostatisticians</li><li>
Global Medical Affairs Scientific Communications personnel</li></ul>
Duties &amp; Responsibilities
People<ul><li>
Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product &ndash; with an objective to develop statistical data outputs</li></ul>
Performance/Process<ul><li>
Conduct appropriate post-hoc statistical analyses of clinical trial data</li><li>
Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS</li><li>
Produce well documented data packages that include tables, listings, and figures</li><li>
Closely follow QC plans and timelines set by senior members of the MedHub biostatistics and programming team</li><li>
Remain current on advanced programming methods</li></ul>
Customer<ul><li>
Work closely with Global Medical Affairs biostatisticians to identify statistical analysis needs and assist in developing assigned deliverables</li></ul>
Knowledge, Skills &amp; Competencies / Language<ul><li>
Stakeholder management</li><li>
Ability to manage timelines</li><li>
Ability to work independently and within a team environment</li><li>
Advanced SAS programming skills</li><li>
Excellent English language knowledge &ndash; written and spoken</li></ul>
Qualifications
<ul><li>Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field</li><li>
Master's degree 0-2 years/B.Sc. 3-6 years of relevant experience required</li></ul>
Requirements of the job
<ul><li>Advanced SAS and other statistical computing software skills in a clinical data environment across multiple therapeutic areas</li><li>
Expertise in the use of data management applications and database/file structures, specifically with respect to CDISC requirements</li><li>
Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines</li><li>
Capacity to respond to unscheduled changes in project workload</li></ul>
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Statistical Programmer

<div>Job title: Senior Scientific Writer &ndash; Health Economics and Value Assessment (HEVA)<ul><li> 
Hiring Manager: Head/Group Lead/Team Lead HEVA</li><li>
Location: Hyderabad</li><li>
% of travel expected: Travel required as per business need</li><li>
Job type: Permanent and Full time</li></ul> 
About the job 
Our Team:
Sanofi Global Hub (SGH) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&amp;D, Data &amp; Digital functions. SGH strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. 
Main responsibilities:
The overall purpose and main responsibilities are listed below:
Create HEVA communications deliverables (including manuscripts, posters, abstracts, slide decks) aligned with HEVA strategy and global HEVA communication plan across relevant business units and product teams. Manage core HEVA communication processes, templates, and products across the portfolio in accordance with the scientific and value messages aligned with Core Value Dossier, the US AMCP Dossier, and HEVA contributions as appropriate to other submissions. Ensure Core Value Decks for key products are established and maintained, making available a regularly updated synthesis of critical HEVA evidence on the value of products. Maintain accountability for adherence to the publication standard operating procedure (SOP) and other compliance expectations relevant to HEVA communication processes. Seek opportunities to innovate HEVA value communications to increase the relevance and impact of HEVA evidence and inform optimal access and reimbursement decisions. Develop and maintain therapeutic area expertise. Coach junior HEVA writers and develop and review content created by them. Manage end to end process through iEnvision (previously, Datavision/Matrix). Collaborate effectively with stakeholders: HEVA, RWE, and Scientific communication global and/or local teams.<ul><li> 
People: (1) Maintain effective relationships with the end stakeholders within the allocated GBU and product &ndash; with an end objective to develop education and communication content as per requirement for HEVA communications; (2) Interact effectively with healthcare professionals on publication content; and (3) Constantly assist other writers (junior) in developing knowledge and sharing learning</li></ul><ul><li> 
Performance: (1) Create HEVA communications deliverables (including manuscripts, posters, abstracts, and slide decks) aligned with HEVA strategy and global HEVA communication plan across relevant business units and product teams as per agreed timelines and quality; and (2) Provide strategic support with individuals and institutions, which may serve as resources for publications purpose, etc</li></ul><ul><li> 
Process: (1) Develop complex publications material; (2) Act as an expert in the field of medical communication for the assigned therapeutic area; (3) Assist the assigned scientific communication team in conducting comprehensive publication-needs analysis; (4) Manage core HEVA communication processes, templates, and products across the portfolio in accordance with the scientific and value messages aligned with Core Value Dossier, the US AMCP Dossier, and HEVA contributions as appropriate to other submissions; (5) Ensure Core Value Decks for key products are established and maintained, making available a regularly updated synthesis of critical HEVA evidence on the value of products; (6) Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes; (7) Maintain accountability for adherence to the publication SOP and other compliance expectations relevant to HEVA communication processes; (8) Implement relevant element of publication plan and associated activities for the year identified for the region; (9) Work with selected vendors within the region to deliver the required deliverables as per defined process; and (10) Design an overall plan of action based on end-user feedback and improve course content and delivery</li></ul><ul><li> 
Stakeholder: (1) Work closely with HEVA global and local teams, RWE global and local teams and scientific communication teams in regions/areas to identify publications needs and assist in developing assigned deliverables; and (2) Liaise with HEVA global and local teams to prepare relevant and customized deliverables</li></ul> 
About you 
<ul><li>Experience: &gt;4 years of experience in content creation for the pharmaceutical/healthcare industry, or academia</li><li>
Soft skills: Stakeholder management; communication skills; and ability to work independently and within a team environment</li><li>
Technical skills: Relevant training/experience in health economics, public health, epidemiology, or other relevant health-related scientific discipline (including but not limited to therapeutic area/domain knowledge exposure; knowledge of Good Publication Practice; publication submission; and/or project management)</li><li>
Education: Advanced degree in life sciences/pharmacy/similar discipline or medical degree</li><li>
Languages: Excellent knowledge of English language (spoken and written)</li></ul> 
Pursue progress, discover extraordinary 
Better is out there. Better medications, better outcomes, better science. But progress doesn&rsquo;t happen without people &ndash; people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let&rsquo;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, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
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Senior Scientific Writer (Health Economics and Value Assessment)

<div>
 
 About Sanofi
 
 
 
 We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people&rsquo;s lives.
 
 
 
 About The Job
 
 
 
 The Regional Treasury Analyst oversees cash operations and treasury activities for their assigned area. This role is responsible for managing bank accounts, payments, netting, and fees. The position involves managing currency exposure, cash repatriation, reporting on cash flow, and participating in finance projects, Regional Treasury Analyst will report directly to Africa Head of Treasury.
 
 
 The Regional Treasury Team serves as a strategic hub managing treasury operations across African markets, delivering comprehensive financial management and risk mitigation solutions. Our Regional Team in Cairo will be organized around a dual approach between country specific and transversal activities to optimize efficiency while maintaining local responsiveness.
 
 
 
 Main Responsibilities
 
 
 
 Cash management and liquidity:
 
 
 <ul>
 <li>
 Execute daily cash position reporting and monitoring across all bank accounts.
 </li>
 <li>
 Process electronic fund transfers, wire payments, and manual disbursements
 </li>
 <li>
 Monitor account balances to ensure adequate funding for operational needs
 
 
 </li>
 </ul>
 
 Trade Finance And Banking Operation
 
 
 
 <ul>
 <li>
 Process and monitor trade finance instruments including LCs, LGs &amp; DCs
 </li>
 <li>
 Review, validate, and reconcile bank fees, interest charges, and service costs
 </li>
 <li>
 Serve as the operational contact for banking partners
 </li>
 <li>
 Coordinate documentation for new account openings and closures
 </li>
 <li>
 Ensure accurate settlement of foreign exchange transactions.
 
 
 </li>
 </ul>
 
 Financial Analysis And Reporting
 
 
 
 <ul>
 <li>
 Analyze working capital metrics including DPO, DIO, and DSO.
 </li>
 <li>
 Develop dashboards and analytics to track key treasury performance indicators
 </li>
 <li>
 Assist in preparing presentations for senior management on treasury activities
 </li>
 <li>
 Document treasury processes and procedures for audit purposes
 
 
 </li>
 </ul>
 
 Risk Management And Compliance
 
 
 
 <ul>
 <li>
 Track and report on interest rate and foreign exchange exposures
 </li>
 <li>
 Ensure compliance with internal control for treasury operations
 </li>
 <li>
 Contribute to Business Continuity Planning (BCP) for treasury functions
 </li>
 <li>
 Monitor compliance with established treasury policies and procedures.
 
 
 </li>
 </ul>
 
 Cross-Functional Collaboration
 
 
 
 <ul>
 <li>
 Coordinate with Accounting team on a timely bank reconciliation and resolve discrepancies.
 </li>
 <li>
 Support month-end closing activities related to treasury transactions.
 
 
 </li>
 </ul>
 
 About You
 
 
 
 
 Education:
 
 Bachelor&rsquo;s degree in business administration, finance, accounting or economics English or French section.
 
 
 
 Related Experience:
 
 +2 years of Treasury experience is preferred for this role. knowledge of cash management and treasury systems and/or accounting and/or financial analysis and/or SAP user.
 
 
 
 Skills
 
 
 
 <ul>
 <li>
 Strong analytical skills, financial acumen, accuracy and attention to details.
 </li>
 <li>
 Ability to build strong working relationships with partners internally and externally with banks; verbal, and written communication skills
 </li>
 <li>
 Team player, proactive and solution oriented
 </li>
 <li>
 Strong capabilities in MS Excel.
 
 
 </li>
 </ul>
 
 Languages:
 
 Strong written and spoken French/ English.
 
 
 
 Why choose us?
 
 
 
 <ul>
 <li>
 Ready to push the limits of what&rsquo;s possible? Join Sanofi in one of our corporate functions and you can play a vital part in the performance of our entire business while helping to make an impact on millions around the world.
 </li>
 <li>
 Make your work count by supporting a company that brings life-changing treatments to millions &mdash; and is committed to doing right by patients, communities, and the planet.
 </li>
 <li>
 Drive progress from within by helping simplify, scale, and modernize how a global biopharma business delivers smarter, faster, and more sustainably.
 </li>
 <li>
 Support teams across science, medicine, and operations by building better systems, shaping bold strategies, and enabling innovation at speed.
 </li>
 <li>
 Make an impact across borders and functions, collaborating with leaders to turn complex challenges into real-world solutions.
 </li>
 <li>
 Advance your career through stretch roles, cross-functional moves, and development opportunities designed to match your ambition.
 </li>
 <li>
 Thrive in inclusive, high-performing teams where every role matters and every voice helps shape what&rsquo;s next.
 
 
 </li>
 </ul>
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</div>

Regional Treasury Analyst (French Speaking countries)

<div>Job title: Project Lead &ndash; RWE Data Analytics<ul><li>Hiring Manager: RWE Lead, Sanofi Business Operations</li><li>Location: Hyderabad</li><li>% of travel expected: Travel required as per business need</li><li>Job type: Permanent and Full time</li></ul>
About the job
Our Team:
Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&amp;D, Data &amp; Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally.
Main responsibilities:
Contribute to the growth of General Medicine&rsquo;s real-world evidence capability, including real world evidence (RWE) to support studies and projects across the franchises motivated by business needs; work closely with the Medical, Market Access, HEOR, and Commercial team to maximize the value of our portfolio of priority assets worldwide; unique opportunity for a data scientist and/or epidemiologist to join a motivated and experienced research team in an innovative working environment to address key tasks in health and social care surrounding CV disease and diabetes; work collaboratively to create high quality innovative analytical products, can benefit from a wealth of in-house databases, study platforms, and analytic tools, and from external partnerships with academic and governmental institutions<ul><li>People:</li></ul>
(1) Work together with RWE team to support projects across the franchises motivated by business needs;
(2) Work closely with the Medical, Market Access, HEOR, and Commercial team to maximize the value of our portfolio of priority assets worldwide;
(3) Work collaboratively within Medical and across functions, with clients and external collaborators;
(4) Functionally reports to the Head of the Real-World Evidence team<ul><li>Process:</li></ul>
(1) Work together and lead research analytical projects, including project conceptualization and design;
(2) Lead analysis of healthcare data, including clinical trial datasets, transactional claims, and electronic health records, using established and novel statistical and analytical techniques;
(3) Generate rapid response analyses for cross-functional stakeholders;
(4) Lead or contribute to drafting and reviewing technical and study reports, manuscripts for publishing in high-impact peer-reviewed journals, and abstracts and presentations for international conferences;
(5) Actively manage project activity and timelines;
(6) Internally advise your colleagues in the Health Economics, Commercial, and Medical franchises on your areas of technical and research expertise as directed by your supervisor;
(7) Communicate complex concepts and interpretation of analysis and findings to different audiences, including health economists, clinicians, policy makers, and health systems;
(8) Represent the team at external meetings;
(9) Validate and secure access to third-party healthcare data-sets<ul><li>Customer:</li></ul>
(1) Deliver research and contributes to the RWE strategic direction for General Medicines
About you<ul><li>Experience: 7 - 10 years in public health, biotechnology and/or pharmaceutical industry; Strong healthcare data analysis expertise, expertise in data analysis techniques, and good understanding of healthcare datasets (EHR, Claims, RCTs), and data structures; Expertise in use of statistical methods to investigate real-world problems (e.g., data modelling, time to event analysis); Advanced experience in preparing, analyzing, and managing large healthcare datasets in interventional and/or non-interventional studies; Experienced in interpreting and presenting complex analyses and findings; Experienced in interpreting and presenting complex analyses and findings</li><li>Soft skills: Integrity; Analytic excellence; Excellent written and oral communication skills; ability to communicate complex topics and data results in a concise and precise manner; High level of self-awareness; Ability to cooperate cross-functionally; Problem-solving and creative thinking skills; Enjoys working independently, flexibly and as part of a team on multiple projects; Enthusiastic and professional approach to working with colleagues, clients, and external collaborators</li><li>Technical skills: R, Python, SQL, advanced Microsoft Excel using Visual Basic for Application, SAS Education: Masters or PhD in a quantitative subject (e.g., computer science, data science, statistics, mathematics, biostatistics, biomedical engineering, epidemiology) or equivalent combination of education, training, and experience</li><li>Languages: Excellent knowledge of English language (spoken and written)</li></ul>
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn&rsquo;t happen without people &ndash; people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let&rsquo;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, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
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RWE Project Lead Analytics

<div>Job title: RWE Scientist<ul><li>Hiring Manager: Head scientific communications, Sanofi Business Operations</li><li>Location: Hyderabad</li><li>% of travel expected: Travel required as per business need</li><li>Job type: Permanent and Full time</li></ul>
About the job
Our Team:
Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&amp;D, Data &amp; Digital functions. Sanofi Business Operations strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally.
Main responsibilities:
The Real-World Evidence (RWE) Investigator is an important scientific position responsible for supporting the development, coordination, and execution of cutting-edge, effective, and efficient real world evidence strategy for drug and enablement projects at global level or for key critical markets. He/she works in close partnership with the global RWE Strategy Therapeutic Area Lead to develop consensus among diverse scientific, technical, and business experts to ensure high scientific rigor and timely, cost-effective study or project delivery while adhering to ethical requirements and responding to business needs.<ul><li>Partner with and support the Real-World Evidence Strategy Lead(s) on the design, execution, analysis, interpretation, and internal and external communication of specific epidemiological/outcomes research studies.</li><li>Provide strategic input, epidemiological/outcomes research support, and leadership to project teams and the RWD&amp;ES Team during all stages of pharmaceutical development to maximize the market potential of products, manage risks, and optimize epidemiological processes and methods.</li><li>Deliver specialized research to enhance the effectiveness of RWE contributions to regulatory submissions and the drug research process including discovery, development, and commercialization across assigned products.</li><li>Support the end-to-end execution of real-world studies ensuring deliverables are on time, within budget, to specification and of high scientific rigor that demonstrates commitment to quality.</li><li>Provide innovative thinking regarding the design of clinical and epidemiological/outcomes research programs that support commercialization.</li><li>Set standards for utilization of real-world evidence, provide methodological leadership and input to real-world evidence strategies.</li><li>Identify and validate external fit-for-purpose data sources, associated institutions and/or organizations, in collaboration with other members of the RWD&amp;ES team.</li><li>Provide support to the Real-World Evidence Team and to the company in a specific epidemiological/outcomes research area of expertise, and typically, in a specific therapy area</li><li>Maintain timely communication and close alignment with team members, partners and stakeholders to ensure clear and timely visibility the evidence strategy, study progress and anticipation of challenges and risk mitigation.</li><li>Work seamlessly with partners and stakeholders to identify solutions in an optimal and efficient manner; synergize and optimize resources and efforts where appropriate.</li></ul>
About you
You are a self-starter who brings your energy, expertise and experience as well as takes an entrepreneurial approach to solving problems, have a growth mindset and are passionate about unleashing the power of real-world data with data science to improve health.
Education:<ul><li>Advanced degree in pharmaco-epidemiology, biostatistics, Health Outcomes, or equivalent discipline.</li></ul>
Experience:<ul><li>Minimum 7 years real-world evidence generation in or for the pharmaceutical industry.</li><li>Knowledge of RWE and its application to support pharmaceutical development, regulatory approval and patient access at an international level.</li><li>Understanding of the product development processes at all stages of the product life cycle to influence the appropriate use of RWE activities.</li><li>Use of innovative RWE methodologies to address evidence gaps.</li><li>Experience working in multiple therapeutic areas &ndash; experience in transplant, type 1/2 diabetes and cardiovascular is highly preferred.</li><li>Cross-functional collaboration and alignment in complex global matrix teams.</li></ul>
Soft skills:<ul><li>Excellent written and verbal communication skills, negotiation and interpersonal skills</li><li>Proven teamwork and collaboration skills</li><li>Well-developed cultural sensitivity</li><li>Strong sense of urgency, ownership and proactive attitude to deliver value to our brands.</li><li>Ability to adapt and communicate messages to a wide range of audiences at all levels (both scientific and commercial), inside and outside of the organization, to convince others of the value of our brands.</li><li>Ability to effectively negotiate and compromise with internal and external stakeholders to achieve optimal results for the business, agile to change, and obtain and manage budgets.</li><li>Apply growth mindset to develop new skills or knowledge.</li></ul>
Technical skills:<ul><li>Demonstrated expertise in pharmacoepidemiology, HEOR and RWE study designs and methodologies, including innovative techniques.</li><li>Experience working with routinely collected data (claims databases, electronic medical health records, registries and various structured and possibly unstructured sources in the healthcare sector within pharmaceutical company settings.</li><li>Ability to translate business needs into study and data requirements.</li><li>Project management of real-world studies and management reporting</li></ul>
Languages:<ul><li>Fluency in spoken and written business English mandatory</li><li>Proficiency or working knowledge of French or other European languages</li></ul>
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But progress doesn&rsquo;t happen without people &ndash; people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let&rsquo;s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
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RWE Scientist

<div>Omnichannel Project Specialist - VIE Contract<ul><li>
Location: United States of America, Cambridge</li><li>
Target start date: 01/05/2026</li></ul>
iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.
PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.
PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English will be considered. Please make sure to apply with your personal email address.
About the job
As Omnichannel Project Specialist VIE within our Marketing team, you&rsquo;ll join our Immunology Alliance team and drive the execution of our comprehensive 2026 Omnichannel Roadmap. 
Kevzara (sarilumab) is Sanofi's innovative treatment for rheumatoid arthritis and other inflammatory conditions, representing a key asset in our Immunology Alliance portfolio. Join us in shaping the future of pharmaceutical marketing and making a real difference in patients' lives through innovative omnichannel approaches and digital excellence.
In Specialty Care, you&rsquo;ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. 
 
Ready to get started? 
About Sanofi
We&rsquo;re an R&amp;D-driven, AI-powered biopharma company committed to improving people&rsquo;s lives and delivering compelling growth. Our deep understanding of the immune system &ndash; and innovative pipeline &ndash; enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people&rsquo;s lives.
Main responsibilities:<ul><li>
Content Management &amp; Localization: Collaborate with US Kevzara marketing team to manage global content repository, lead content repurposing and adaptation initiatives, and implement unified Veeva Portal operations with GenAI-powered content creation.</li><li>
SEO/GEO Strategy Implementation: Evaluate unbranded global website development needs with best-in-class Search Engine Optimization / Generative Engine Optimization (SEO/GEO) optimization and assess potential for global deployment with country-specific capabilities.</li><li>
Cross-Functional Collaboration: Create and manage country team lists, facilitate meetings with key markets (US, Germany), and define Global team formation and governance.</li></ul>
About you
Experience:<ul><li>
2+ years of pharmaceutical marketing or omnichannel strategy experience.</li><li>
Proven experience with content management systems (Veeva Vault, SFMC) and strong understanding of SEO/GEO strategies.</li></ul>
Soft and Technical skills:<ul><li>
Excellent project management skills with ability to manage multiple initiatives and strong cross-functional collaboration abilities.</li><li>
Experience with AI-powered content creation and localization tools would be preferred.</li><li>
Previous experience in global pharmaceutical companies with certification in digital marketing or project management would be preferred.</li><li>
Experience with Salesforce Marketing Cloud and Customer Relationship Management (CRM) platforms would be preferred.</li><li>
Ability to develop and execute comprehensive omnichannel strategies aligned with business objectives.</li><li>
Deep understanding of digital marketing technologies, platforms, and emerging trends.</li><li>
Strong written and verbal communication skills for diverse stakeholder audiences with ability to adapt quickly to changing priorities.</li></ul>
Education:<ul><li>
Bachelor's degree in Marketing, Business Administration, Life Sciences, or related field.</li></ul>
Languages:<ul><li>
Fluent English (written and verbal).</li></ul>
Why choose us?<ul><li>
Be part of a pioneering biopharma company where patient insights shape drug development.</li><li>
Work at the forefront of AI-powered science that accelerates discovery and improves outcomes.</li><li>
Collaborate beyond your expertise, sparking new ideas with diverse, multidisciplinary teams.</li><li>
Work in a place that combines global scale with local expertise, backed by a strong culture of collaboration and shared purpose.</li><li>
Contribute to innovations that improve outcomes, relieve pressure on healthcare systems, and expand access worldwide.</li><li>
Join a team that&rsquo;s not just transforming treatment - but asking what&rsquo;s next, and making it real.</li><li>
Be part of a simpler, digital- and AI-powered business that&rsquo;s rethinking how we work and engage with the world.</li></ul>
iMove is a unique program tailored for European youth interested in challenging themselves with meaningful assignments across the globe. At Sanofi we have a strong ambition to invest in young talents who will drive the success of Sanofi tomorrow.
Sanofi&rsquo;s Work Abroad Program, iMove, offers jobs-assignments with actual responsibilities and a perspective to grow. We provide those opportunities in various functions such as: marketing, finance, regulatory, supply chain, clinical trials, production, etc. and in more than 40 countries. Sanofi unites people who are passionate about solving healthcare needs across the world. Joining our iMove Work Abroad Program is a unique opportunity to make a difference through your work.
#LI-EUR
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Omnichannel Project Specialist - VIE Contract

Join Sanofi and explore 11   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.