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121201 F. Hoffmann-La Roche AG

Clinical Supply Chain Lead(m/w/x)

Kaiseraugst
Full-timeOn-siteSenior

At a global pharmaceutical company, clinical supply chain planning for Investigational Medicinal Products (IMPs) using SAP/APO/OMP and CLARA. 5+ years in supply chain planning for clinical trials, with ERP system experience (SAP, OMP, APO) and IRT, required. Cross-functional collaboration with Technical Development and Clinical Core Teams.

Requirements

  • Academic degree or equivalent diploma in Life Sciences, Business, or Engineering
  • 5+ years of related experience in Clinical Supply Chain, Planning, Manufacturing, or similar discipline
  • 4+ years of experience with a Master's Degree
  • Solid understanding of clinical trial design, drug technical development, demand forecasting, and supply planning techniques
  • ERP system experience (e.g., SAP, OMP, or APO) and IRT
  • Strong knowledge of GMP manufacturing, quality assurance, regulatory affairs, and budget planning
  • Proven ability to lead process improvement activities
  • Ownership of various Clinical Supply Chain business processes
  • Excellent verbal/written communication and presentation skills
  • Strong analytical, logic, and problem-solving skills
  • Advanced knowledge of Excel
  • Detail-oriented with strong planning skills
  • Experience in project management within a cross-functional and cross-cultural environment
  • Excellent written and oral communication in English
  • German language skills may be a plus

Tasks

  • Own demand and supply planning for all IMPs in SAP/APO/OMP and CLARA
  • Adjust Demand and Supply Plans based on Clinical Operations assumptions
  • Analyze risks, costs, and feasibility proactively
  • Serve as the primary contact for clinical supply topics
  • Collaborate with Technical Development Teams and Clinical Core Teams
  • Ensure alignment of activities and timelines across cross-functional teams
  • Maintain oversight on performance and issue resolution
  • Optimize the supply chain using simulation techniques
  • Recommend study design characteristics to support supply chain optimization
  • Manage drug supply-related budget planning for IMP
  • Incorporate regulatory and quality requirements into the supply plan
  • Act as a stakeholder manager for the Technical Development Team
  • Align with the molecule Clinical Development Plan

Work Experience

  • 5 years

Education

  • Bachelor's degreeOR
  • Master's degree

Languages

  • EnglishBusiness Fluent
  • GermanBasic

Tools & Technologies

  • SAP
  • OMP
  • APO
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