Director CTSM, Supply & Data Integration

BioNTech AG
München, Germany
13 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Working hours
Shift work
Languages
English, German

Tech stack

Information Systems Data Governance Data Integration Data Integrity Data Flow Control SAP (Applications) SAP Business Suiteing Product Software Implementation Methods Data Streaming Expertise in Kinaxis Information Technology SAP S/4HANA
+2 more
Data Management Veeva

Job description

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. Your Contribution:

  • 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

Requirements

  • 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; experience with system providers is an advantage
  • 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
  • Advanced experience integrating diverse data flows while managing administrative functions for data flow control and access across systems supporting clinical trial supply activities
  • 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

Benefits & conditions

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

About the company

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. Inspired? Become part of #TeamBioNTech. BioNTech, the story At BioNTech, we are more than just a biotechnology company - we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases. Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine. Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world. BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you! BioNTech - As unique as you

Apply for this position

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