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BioNTech is seeking a Manager CTSM Supply & Data Integration to deploy, configure and optimize the SAP-based CTSM ecosystem across global trials. You will partner with IT and business teams to ensure data accuracy and seamless system integrations in a fast-paced, regulated environment.
Ideal candidates have a university degree in a relevant field and at least 3 years in Clinical Trial Supply Management, with hands-on SAP/S4HANA and data integration experience.
Mainz, Germany; London, United Kingdom; Munich, Germany | full time | Job ID:11623
As Manager CTSM Supply & Data Integration, you will play a critical role in deploying, configuring and optimizing BioNTech's Intelligent Clinical Supply Management (ICSM) SAP module within our global Clinical Trial Supply Management (CTSM) division. Acting as a key counterpart to IT, you will help ensure seamless data flow and accuracy across clinical trials while contributing to innovative supply chain solutions. Your work will directly support BioNTech’s mission of delivering therapies that transform lives by advancing our clinical trial capabilities.
In this role, you will collaborate with cross-functional teams and external partners to streamline processes, integrate cutting‑edge systems, and enhance data reliability. Join us in an agile and dynamic environment where your expertise will make a difference every day.
Support the deployment and optimization of the CTSM digital ecosystem, including ICT and its integration with systems such as S/4HANA, IRT, and vendor platforms
Collaborate with the CTSM Global Template Process Owner by aligning SAP value streams (e.g., I2R, S2S, MDM) with business needs through cross-functional collaboration
Identify ICT/SAP workflow requirements while harmonizing business needs with system capabilities for efficient execution
Act as the business process owner representative for SAP/ICSM system URS validation processes
Manage projects related to CTSM master data and integration; resolve issues, implement data governance practices, and optimize processes during transformations
Completed university degree in Engineering, Clinical Supply Chain Management, Quality Management, Computer Science, Information Systems, or related field
Minimum 3 years of experience in Clinical Trial Supply Management within pharmaceutical/biotech or regulated industries; experience with system providers is an advantage
Expertise in ERP/IT implementation projects such as SAP S/4HANA; familiarity with ICTM modules and third-party data integration concepts
Proven skills in executing SAP-supported clinical supply processes like material management, demand/supply planning, and logistics using tools like Kinaxis, ICTM, IRT or Veeva
Strong project management abilities paired with excellent organizational and communication skills for stakeholder engagement
Fluency in English (business-professional level); German proficiency is highly desirable
It's our priority to support you:
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
Job ID 11623(please always specify if you have any questions)
By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.