Job
In dieser Rolle entwickelst du Lösungen für die Implementierung und Optimierung des ICSM SAP-Moduls, führst Datenintegrationsprojekte durch und steuerst Prozesse im Bereich klinischer Studienversorgung.
Job-Technologien
Deine Rolle im Team
- As Associate Director CTSM Supply & Data Integration, you will lead the deployment, configuration, and optimization of BioNTech's Intelligent Clinical Supply Management (ICSM) SAP module within our global Clinical Trial Supply Management (CTSM) division.
- Acting as a strategic counterpart to IT, you will ensure seamless data flow, accuracy of information, and optimized processes across clinical trials and external partners.
- In this role, you will collaborate with cross-functional stakeholders to drive innovation in clinical supply chain management.
- Your expertise will directly contribute to advancing BioNTech's mission of delivering transformative therapies while setting new standards in clinical trial supply management.
- Act as Business Process Owner for assigned workstreams within the CTSM digital ecosystem, including ICSM integration with systems such as S/4HANA, IRT, and vendor platforms; oversee rollout, change management, and training initiatives.
- Serve as CTSM Global Template Process Owner for SAP value streams (e.g., I2R, S2S, MDM), ensuring alignment with business needs through collaboration with template process owners and system stakeholders.
- Lead the identification and alignment of ICSM/SAP workflow requirements while managing expectations for harmonized execution of business requirements and system capabilities.
- Represent CTSM as Business Owner for SAP/ICSM system URS validation processes.
- Lead projects related to CTSM master data and integration; resolve issues, implement data governance practices, optimize processes during transformations, and enhance data reliability.
Unsere Erwartungen an dich
Ausbildung
- Completed university degree in Engineering, Clinical Supply Chain Management, Quality Management, Computer Science, Information Systems, or a related field (Doctorate preferred).
Qualifikationen
- Proven Track record with Clinical Trial Supply Management activities and supporting systems such as Kinaxis, ICSM, IRT or Veeva.
- Excellent project management skills paired with strategic thinking and negotiation abilities.
- Fluency in English (business-professional level); German proficiency is highly desirable.
- Ability to lead various individuals of different professional backgrounds and expertise levels toward shared goals.
Erfahrung
- Minimum 5 years of experience in Clinical Trial Supply Management within pharmaceutical/biotech or regulated industries; experience with system providers is an advantage.
- Experience in ERP/IT implementation projects such as SAP S/4HANA, ICSM module including third-party data integration concepts.
- Advanced experience integrating diverse data flows while managing administrative functions for data flow control and access across systems supporting clinical trial supply activities.
Unser Angebot
- Your flexibility: flexible hours | vacation account.
- Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning.
- Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential.
- Your health and lifestyle: Company bike.
- Your mobility: Job ticket | Deutschlandticket.
- Your life phases: Employer-funded pension | Childcare.
Benefits
Work-Life-Integration
Themen, mit denen du dich im Job beschäftigst
Job-Standorte
Das ist dein Arbeitgeber
BioNTech ist ein Immuntherapie-Unternehmen, das bei der Entwicklung von Therapien für Krebs, Infektionskrankheiten und seltene Erkrankungen Pionierarbeit leistet. Das Unternehmen kombiniert Immunologieforschung, moderne therapeutische Plattformen und Bioinformatik-Tools, um die Entwicklung neuartiger Biopharmazeutika rasch voranzutreiben.
- 250+ Mitarbeitende
- 2008
- Etablierte Firma
- Onsite, Hybrid
- Pharma, Chemie, Biotech
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