Clinical Supply Optimization Specialist

Sanofi • Morristown, NJ

5d • Onsite

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 Optimization Specialist (CSOS) 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

• Identify the best strategy/settings for an optimized study design with strong impact on study budget and design
• Support and review all IRT set-up and treatment number list structure for medium and complex designs
• Promote strong relationships with external and internal experts (N-Side, IRT gov, IRT ref, IRT L2 and IRT providers)
• Contribute to governance activities including annual objectives related to Technology, budget monitoring and metrics analysis
• Lead process improvement, Quality Document updates and user training
• Ensure clear, concise, consistent and timely communication across CSCO functions and within CSO

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees