Interim Business Intelligence Partner (Germany) Role Purpose Act as the executive partner to the German site to design, govern, and deliver the digital, data, and AI portfolio that underpins product launches and omnichannel excellence in Germany. You will own the local BIS strategy-to-execution, align it with global/regional platforms, and lead a multi-vendor ecosystem (incl. Veeva CRM & Veeva Vault MedComms/PromoMats) to measurable commercial and medical outcomes—fully compliant with GDPR/GxP and local codes. What You’ll Lead Strategy & Operating Model: Define the Germany BIS agenda (Commercial & Medical), target architecture, and investment roadmap; establish program governance, KPIs/OKRs, and risk/compliance controls. Enterprise Platforms at Scale: Direct the enterprise-level adoption of Veeva CRM and Vault (MedComms/PromoMats), consent and identity, content supply chain/MLR, and field effectiveness tooling; ensure interoperability with analytics, data platforms, and SAP/ERP/MDM. Data & AI for Decisions: Industrialize data products and advanced analytics (e.g., next-best-action, segmentation, field performance, medical engagement insights). Set standards for responsible AI and model lifecycle governance. Change & Value Realization: Drive executive stakeholder alignment, field adoption, and benefit tracking for launches and lifecycle brands; coach local leaders and global partners to embed new ways of working. Vendor & Portfolio Leadership: Lead SI/consulting partners, negotiate scope and commercials, and manage a multi-million EUR portfolio to time, budget, and outcomes. Profile (Must-Have) 10 years in Life Sciences IT/Digital, including 5–8 years at Manager/Director/Head/VP level owning Commercial &/or Medical BIS in Germany or EU. End-to-end ownership of Veeva CRM & Vault (MedComms/PromoMats) at country/cluster or regional scale —not just a project workstream. Proven leadership of Germany product launches/omnichannel programs with quantifiable impact (e.g., time-to-approval, MLR cycle time, field productivity, adoption). Budget & vendor management for multi-partner portfolios; has negotiated complex MSAs/SOWs and driven value realization. Deep command of GDPR, consent, GxP, and MLR processes; knows how to operationalize them in tooling and data flows. Hands-on with data & AI enablement for field/medical (NBA/NBO, content personalization, insights generation) and the associated governance. German and English fluent. Executive stakeholder management (GM/Medical/Commercial leads, Global/Regional Tech). Background may include top-tier consulting or prior Head of Commercial IT / Head of Medical IS in biopharma. Nice to Have Experience rolling out responsible GenAI for Med/Commercial (e.g., medical content drafting/QA, rep assist, insight summarization). Integration depth across SAP/ERP, MDM, Identity/Consent, CDP/DWH/Lakehouse, and marketing automation ecosystems. Track record improving MLR throughput and content supply chain with metrics. Location: Germany Industry: Biopharmaceuticals Contract: Freelance / Payroll - 1 year Start Date: Asap