Job
- Level
- Lead
- Job Feld
- BI, Project
- Anstellung
- Vollzeit
- Vertragsart
- Unbefristetes Dienstverhältnis
- Ort
- Mainz
- Arbeitsmodell
- Onsite
Job Zusammenfassung
In dieser Rolle führst du den Rollout und die Optimierung des SAP ICSM-Moduls für die klinische Versorgung und Datenintegration durch, arbeitest eng mit verschiedenen Stakeholdern zusammen und leitest Projekte zur Verbesserung von Datenflüssen und Prozessen im klinischen Umfeld.
Job Technologien
Deine Rolle im Team
- As 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 pivotal leadership 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 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.
- Direct 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 in ERP/IT implementation projects such as SAP S/4HANA; expertise in ICSM modules and third-party data integration concepts.
- Demonstrated skills as a super user overseeing SAP-supported clinical supply processes like material management, demand/supply planning, and logistics using tools such as Kinaxis, ICSM, IRT or Veeva.
- Exceptional project management skills paired with strategic thinking and negotiation abilities; adept at making decisions that prioritize team success.
- Fluency in English (business-professional level); German proficiency is highly desirable.
- Strong leadership abilities to guide individuals with diverse professional backgrounds 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.
- 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
Mehr Netto
Themen mit denen du dich im Job beschäftigst
Job Standorte
Das ist dein Arbeitgeber
BioNTech AG
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.
Description
- Unternehmensgröße
- 250+ Employees
- Gründungsjahr
- 2008
- Unternehmenstyp
- Etablierte Firma
- Arbeitsmodell
- Hybrid, Onsite
- Branche
- Pharma, Chemie, Biotech
Director CTSM, Supply & Data Integration
- Ort
- Mainz
- Arbeitsmodell
- Onsite
- Diversität
- Für alle Personen geeignet (m/w/d)
