About The Position

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. Take part of the Sanofi Research & Development organization and join our Clinical Supply Chain Project Management (CSC-PM) department within Clinical Supply Chain Operations (CSCO), which ensures that supplies needed to conduct any Sanofi Pharma and Vaccines clinical trial are set up, planned, ordered, packed and delivered in more than 80 countries so that trial implementation is not disrupted. As a Clinical Supply Chain Simulation and Digital Systems Specialist within the CSC-PM team, you will be accountable to identify an optimized study design to support the best supply strategy and propose disruptive/innovative approaches to improve study/project costs and lead times. You will report to the Clinical Supply Optimization Specialist Leader. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Requirements

  • 5+ years' experience in pharmaceutical business required with previous experience in supply chain management and forecasting
  • Bachelor's degree – (engineer, PhD, Pharmacist preferred)
  • Deep knowledge of IRT settings and forecasting, risk management, high stake presentation skills, strong ability to analyze data
  • English required, bilingual French preferred
  • Strong leadership, excellent negotiation skills, problem-solving abilities, collaborative mindset

Responsibilities

  • Clinical Supply Forecasting & Simulation
  • Design and implement optimized clinical supply strategies using Monte Carlo simulation methodologies to minimize study costs and enhance operational efficiency
  • Leverage advanced forecasting models to identify optimal study designs with significant impact on budget optimization and supply chain performance
  • IRT Systems Optimization
  • Lead the setup, configuration and review of Interactive Response Technology (IRT) systems for medium to complex clinical trial designs
  • Optimize treatment randomization structures and supply allocation algorithms to maximize IRT system efficiency
  • Collaborate with IRT governance teams, reference users and external providers to drive best practices
  • Digital Systems & Technology Enhancement
  • Identify and prioritize system enhancements and new functionalities with simulation platform experts (N-Side) and IRT providers
  • Drive the integration of improvement requirements into provider roadmaps to advance clinical supply chain digital capabilities
  • Contribute to technology governance including annual digital roadmap objectives, budget monitoring and performance metrics analysis
  • Champion the adoption of innovative digital tools and methodologies across clinical supply operations
  • Process Excellence & Knowledge Management
  • Drive continuous improvement initiatives and update quality documentation to reflect evolving digital capabilities
  • Develop and deliver training programs on simulation tools, IRT systems and optimization methodologies
  • Ensure clear, consistent and timely communication of digital solutions and best practices across CSCO functions and Clinical Supply Operations

Benefits

  • Bring the miracles of science to life alongside a supportive, future-focused team.
  • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
  • Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

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What This Job Offers

Job Type

Full-time

Career Level

Mid Level

Number of Employees

5,001-10,000 employees

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