Director CTSM, Supply & Data Integration

Stellenbeschreibung:

Overview

As Director CTSM Supply & Data Integration, you will lead the deployment and optimization of the ICSM SAP module within BioNTech’s CTSM division, ensuring data accuracy and efficient processes across trials and partners. You will partner with IT and cross-functional teams to drive innovations in clinical supply management and data flows. This role blends strategic ownership with hands-on governance, shaping how CTSM systems enable scalable, reliable operations. You will contribute to BioNTech’s mission by advancing trial supply excellence and data-driven decision making.

Leistungen / Benefits
  • flexible hours
  • vacation account
  • digital learning
  • leadership development
  • company bike
  • pension (employer-funded)
Verantwortungsbereiche
  • Act as Business Process Owner for the CTSM digital ecosystem, overseeing ICSM integration with systems such as S/4HANA, IRT, and vendor platforms; manage rollout, change management, and training
  • Serve as CTSM Global Template Process Owner for SAP value streams (e.g., I2R, S2S, MDM); align with business needs with template owners and stakeholders
  • Lead identification and alignment of ICSM/SAP workflow requirements, ensuring 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; implement data governance practices to enhance data reliability during transformations
Zentrale Anforderungen
  • Completed university degree in Engineering, Clinical Supply Chain Management, Quality Management, Computer Science, Information Systems, or a related field (Doctorate preferred)
  • Minimum 5 years of experience in Clinical Trial Supply Management within pharmaceutical/biotech or regulated industries
  • Proven ERP/IT implementation experience such as SAP S/4HANA; expertise in ICSM modules and third-party data integration
  • Demonstrated super user experience overseeing SAP-supported clinical supply processes (material management, demand/supply planning, logistics) using Kinaxis, ICSM, IRT or Veeva
  • Advanced experience integrating diverse data flows and managing data governance across systems supporting clinical trial supply activities
  • Exceptional project management, strategic thinking, and negotiation abilities
  • Fluency in English; German proficiency is highly desirable
  • Strong leadership to guide diverse teams toward shared goals
  • leadership
  • strategic thinking
  • negotiation
  • SAP S/4HANA
  • ICSM
  • ERP implementation
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Stelleninformationen

  • Veröffentlichungsdatum:

    14 Sep 2026
  • Standort:

    Mainz
  • Typ:

    Vollzeit
  • Arbeitsmodell:

    Vor Ort
  • Kategorie:

  • Erfahrung:

    2+ years
  • Arbeitsverhältnis:

    Angestellt

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