Job
In this role, you will develop solutions for the implementation and optimization of the ICSM SAP module, execute data integration projects, and manage processes in clinical trial supply management.
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Job technologies
Your role in the 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.
Our expectations of you
Education
- Abschluss eines Hochschulstudiums in Engineering, Clinical Supply Chain Management, Qualitätsmanagement, Informatik, Informationssysteme oder einem verwandten Fachgebiet (Promotion bevorzugt).
Qualifications
- 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.
Experience
- 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.
What we offer
- 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
Higher take-home pay
Topics you will work on
Job locations
About your employer
BioNTech is a cutting-edge immunotherapy company that is leading the way in developing new treatments for cancer, infectious diseases, and rare conditions. The company combines immunology research, modern therapeutic platforms, and bioinformatics tools to quickly develop new biopharmaceuticals.
- 250+ Employees
- 2008
- Established Company
- Onsite, Hybrid
- Pharmaceutical Sector, Chemical Industry, Biotech
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