R&D
Là où votre curiosité fait avancer les miracles de la science
Global Supply Support Team Leader
En bref
Mettez votre curiosité au service d’une équipe où l’immunoscience de pointe rencontre l’innovation la plus avancée. Dans les domaines de l’oncologie, des maladies rares, de la neurologie et des vaccins, vous travaillerez à l’intersection entre la recherche en laboratoire et la découverte boostée par l’IA, tout en collaborant au-delà des frontières pour transformer des idées novatrices en impacts concrets. Que vous souhaitiez approfondir votre expertise scientifique ou évoluer en tant que leader, vous trouverez ici l’opportunité de le faire.
About the job
Our Team:
At Sanofi R&D, we develop future medicines that improve patients' lives worldwide. R&D Supply is managed in collaboration by 3 departments: Clinical Supply Chain Operation (CSCO), Chemistry, Manufacturing and Controls (CMC) and Global Quality Operation (GQO). Those 3 departments include key roles who are responsible to manage supply flow to patients globally for clinical testing according to quality requirements. The Supply Support Team Leader leads a team of diverse roles (depending on the location) including Global Supply Study Supports (GSSS), Investigational Product Supports (IPS), CMC Material & Documentation Flow manager and Temperature excursion Quality manager who provides support on supply activities that can be centralized to a worldwide team. Activities must be done ensuring quality, timely delivery, regulatory compliance, and with an accurate tracking through our internal systems.
The Global Supply Support Team Leader serves as the primary liaison to global functional heads on business topics such as metrics, prioritization, and performance and reports to:
- In Hungary:
- Direct reporting line: to the CSO Study Management Head (HU)
- Functional reporting lines to: HUB Coordinator for CSCO, Clinical Supplies Quality Manager for GQO & Head of Demand & Supply for CMC
- In India:
- Direct reporting line: to the Clinical Study Support Head (India)
- Functional reporting line: to Clinical Supply Chain International Management and HUB Coordinator
Main responsibilities:
- Clinical Trial & Supply Knowledge: Understand clinical trial design, protocols, and regulatory requirements (GxP)
- Manage investigational product lifecycle: kit types, shelf life, production planning, depot management, distribution, reconciliation, and returns/destruction
- Apply knowledge of clinical endpoints, randomization, dosing regimens, cohort management, and stratification factors
- Team Leadership & People Management: Lead, coach, and develop team members through clear direction and targeted training
- Conduct performance reviews, set objectives, and support career development and well-being
- Foster Sanofi's culture of open communication, collaboration, and recognition
- Ensure team qualification, expertise development, and effective onboarding
- Operational Management: Optimize workload distribution and resource allocation across the team
- Oversee planning aligned with study timelines and milestones
- Align team objectives with organizational goals and develop action plans
- Stakeholder Collaboration & Communication Build and maintain relationships with key internal and external stakeholders
- Collaborate closely with CSCO, GQO, and CMC to ensure alignment on goals and ways of working
- Provide regular status updates, KPIs, and analysis of cross-project trends and risks
- Ensure timely information flow and escalate critical issues
- Problem Resolution & Continuous Improvement: Proactively identify and resolve issues, risks, and systemic challenges
- Drive process optimization, standardization, and innovation for efficiency gains
- Implement corrective actions for audit findings and operational issues
- Location-Specific Responsibilities depending on roles to oversee: IPS (Investigational Product Services) Provide expertise and support on temperature excursion, import license, study RFP for distribution provider, reconciliation and any other new activities identified as IPS responsibility.
- GSSS (Global Suply Study Support): Provide expertise and support:
- On IMP transfers to depot in IRT, Inventory Product Stock Management (IPSM) tracker, destruction of expired IMP and AxMP throughout the study lifecycle, reconciliation, monitoring IRT interface failures with Sanofi supply tools, accurately capturing supply plans in Sanofi Clinical Supplies tools (ERP)
- Preparing and maintaining mandatory shipment documentation prior shipment preparation, in filing and archiving IMP-related documents, in preparation for regulatory inspections
- In monitoring IMP and AxMP stock levels throughout the study, tracking shipments throughout the study duration,
- In managing service provider purchase orders and invoices, ensuring regular financial tracking and compliance.
- GQO (Global Quality Operations) :
- Acts as a backup of the Temperature Excursion Manager. As such, ensures activity coverage during Temperature Excursion Manager out-of-office periods
- Provides directions on product acceptability for use in cases where temperature is outside the limits of stability statement
- Ensure temperature excursion management complies with Good Practices (GxP) and Sanofi procedures
- Serve as the Key Expert User for TEX (temperature excursion management and recording)
- Material & Documentation Flow Management: Oversee the management of on/off boarding of external resources
- Oversee the management of training environment and systems
- Oversee the management of documentation and the coordination of products (Drug Products and Marketed Products) receipt and transfer to support supplies delivery
About you
- Experience: 7+ years’ experience in the pharmaceutical/CRO industry in clinical operations/ development with at least 2 years of people management or team coordination
- Technical skills: High level of knowledge in clinical operations focus on supply chain flow.
- Experience in Quality field and knowledge in in GxP regulations is a plus.
- GMP certified
- Experience in Project management
- Ability to navigate in several tools: ERP, Documents management, recording tool, Power BI/App, etc
- Familiarity with TEX (temperature excursion management and recording tool) and document management tools: VeevaVault (QualiPSO), Veeva RIM
- Soft Skills: Result oriented
- Ability to work productively with a broad and diverse group of stakeholders
- Autonomy and proactivity; ability to prioritize tasks
- Collaborative leadership
- Excellent oral and written communication skills
- Education: B.Sc. in Life Sciences (or equivalent)
- Languages: Strong English skills (verbal and written), able to exchange fluently in a global environment
Toujours Progresser. Découvrir l’Extraordinaire.
Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.
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Pourquoi nous rejoindre ?
- Élargissez vos horizons. Grandissez grâce à votre curiosité, avec le soutien nécessaire pour évoluer, apprendre et progresser dans une culture qui valorise le mentorat, la mobilité et le développement ambitieux.
- Accélérez les résultats grâce à la technologie. Exploitez la puissance de l'IA et de l'automatisation pour repousser les frontières de la science et réinventer ce qui est possible en matière de découverte de médicaments.
- Agissez grâce à une innovation inclusive. Contribuez à une science meilleure et à des résultats plus équitables en favorisant une recherche inclusive qui touche plus de personnes, de manière plus significative.
- Transformez les besoins des patients en avancées scientifiques. Faites naître des percées scientifiques qui partent des besoins des patients, et aboutissent à des traitements qui changent des vies.
Rencontrez Nils Libert, Associate Scientist
Faites la connaissance de Nils Libert, Associate Scientist en Belgique, où il joue un rôle clé dans l’avancement de recherches de pointe. Découvrez comment son travail contribue à faire progresser l’innovation, à ouvrir de nouvelles perspectives scientifiques et à développer des traitements qui changent la vie des patients partout dans le monde.
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Nos domaines de recherche prioritaires
Découvrez comment nous réinventons l’avenir de la médecine grâce à l'immunologie, ouvrant la voie à des avancées transversales audacieuses, encore inimaginables il y a dix ans.
Rencontrez nos équipes dans les laboratoires
Poussez les portes de nos labos et écoutez les témoignages scientifiques qui transforment une science de pointe en impact réel, guidés par la curiosité, la collaboration et le sens du collectif.
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