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Manager, CTSM, Supply & Data Integration
BioNTech SEManager CTSM optimizing BioNTech's Clinical Supply Management SAP module within the global Clinical Trial Supply Management division. Collaborating on innovative supply chain solutions enhancing data reliability.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Trial Supply Management and SAP S/4HANA implementation, with a strong focus on optimizing processes and managing data governance in regulated industries. Proven ability to collaborate cross-functionally and engage stakeholders effectively.
Highest-signal resume keywords
Clinical Trial Supply ManagementSAP S/4HANA ImplementationProject ManagementData Governance PracticesStakeholder Engagement
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
ERP ImplementationICSM ModulesMaterial ManagementDemand/Supply PlanningLogistics
Soft Skills
Organizational SkillsCommunication Skills
Tools & Technologies
KinaxisIRTVeeva
Industry Keywords
PharmaceuticalBiotechRegulated Industries
Tech Stack
Tools & technologiesERP
About the role
Key responsibilities & impact- Support the deployment and optimization of the CTSM digital ecosystem, including ICSM 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 ICSM/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
Requirements
What you’ll need- 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 ICSM 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, ICSM, 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.
Benefits
Comp & perks- flexible hours
- vacation account
- Digital Learning
- Performance & talent development
- leadership development
- Apprenticeships
- LinkedIn Learning
- Your voice at the table
- Culture on an equal footing
- Opportunities to shape & impact
- Support for your full potential
- Company bike
- Job ticket
- Deutschlandticket
- Employer-funded pension
- Childcare