Director, Supply & Data Integration

BioNTech SE

Director of Supply & Data Integration at BioNTech overseeing clinical trial supply and data integration. Leading deployment of SAP module and collaborating with stakeholders for innovative solutions.

Posted 7/29/2026full-timeLondon • 🇬🇧 United KingdomLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Trial Supply Management and SAP S/4HANA implementation, with a strong focus on data integration, process optimization, and project management. Proven ability to lead cross-functional teams and drive innovation in clinical supply chain management.

Highest-signal resume keywords

SAP S/4HANA ImplementationClinical Trial Supply ManagementICSM Module ExpertiseProject ManagementData Integration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Supply Chain ManagementERP ImplementationData GovernanceMaterial ManagementDemand/Supply PlanningLogisticsData Flow ControlProcess OptimizationChange ManagementTraining Initiatives

Soft Skills

LeadershipStrategic ThinkingNegotiationCollaborationProblem Solving

Tools & Technologies

KinaxisICSMIRTVeevaS/4HANA

Industry Keywords

PharmaceuticalBiotechRegulated IndustriesClinical TrialsDigital Ecosystem

Tech Stack

Tools & technologies

ERP

About the role

Key responsibilities & impact

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
Ensure seamless data flow, accuracy of information, and optimized processes across clinical trials and external partners
Collaborate with cross-functional stakeholders to drive innovation in clinical supply chain management
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
Lead the identification and alignment of ICSM/SAP workflow requirements
Direct projects related to CTSM master data and integration; resolve issues, implement data governance practices, optimize processes during transformations, and enhance data reliability

Requirements

What you’ll need

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 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
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

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