Role Summary
Clinical Supply Optimization Specialist (CSOS) within the CSC-PM team 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. Reports to the Clinical Supply Optimization Specialist Leader.
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
Qualifications
- Required: 5+ years' experience in pharmaceutical business with previous experience in supply chain management and forecasting
- Required: Bachelor's degree – (engineer, PhD, Pharmacist preferred)
- Required: Deep knowledge of IRT settings and forecasting, risk management, high stake presentation skills, strong ability to analyze data
- Required: English; bilingual French preferred
- Required: Strong leadership, excellent negotiation skills, problem-solving abilities, collaborative mindset
Skills
- Supply chain management
- Forecasting and data analysis
- IRT settings and treatment number list structures
- Governance and metrics analysis
- Stakeholder management and communication
Education
- Bachelor's degree – engineer, PhD, or Pharmacist preferred
Additional Requirements
- None explicitly listed beyond the above; travel or physical demands not specified as essential in the provided description