Clinical Supply Chain Leader

Roche • Mississauga, ON

6d • Onsite

About The Position

At Roche, we foster a culture where individuals are embraced for their unique qualities, encouraging personal expression, open dialogue, and genuine connections. We are a global healthcare leader dedicated to improving patient lives through groundbreaking medicines and diagnostic tools. With over 125 years of heritage, we are committed to sustainable healthcare and addressing complex global health challenges. Our Global Clinical Supply Chain Organization is crucial for our clinical research, ensuring timely patient treatment and trial progression. This role is part of a newly expanded team in Mississauga, Canada, a strategic hub promoting agility, collaboration, and the delivery of life-saving biopharmaceuticals for numerous molecules and clinical trials worldwide.

Requirements

• Minimum of five years of experience in Clinical Supply Chain, Planning, or Manufacturing, ideally within the Biotechnology or Pharmaceutical industry.
• Academic degree in Life Sciences, Business, or Engineering.
• Solid understanding of clinical trial design and drug technical development.
• Skilled at navigating ERP systems and IRT functionalities to manage complex inventory and supply chain optimization simulations.
• High level of proficiency in GMP environments, with a keen eye for quality assurance, regulatory affairs, and budget planning.
• Confident stakeholder manager who excels at building customer focus and earning respect through impactful, needs-driven actions.
• Agile mindset, showing a willingness to experiment with new ideas and lead process improvement activities in a self-directed team environment.
• Action-oriented professional with the ability to influence others, make decisive choices.
• Ability to travel internationally to support global operations.

Responsibilities

• Take ownership of the clinical study supply chain for Investigational Medicinal Products (IMP), ensuring effective and cost-conscious delivery across diverse disease areas.
• Execute end-to-end demand and supply planning within ERP systems, such as SAP, to maintain robust aggregate and long-range program oversight.
• Lead the alignment of key activities and timelines across cross-functional teams to ensure every clinical trial is supplied in strict accordance with agreed scopes.
• Strategically forecast, plan, and initiate the procurement of comparator drugs and other study materials required for complex clinical protocols.
• Integrate all relevant regulatory and quality requirements into the supply plan to ensure compliance with international standards and GMP environments.
• Drive business excellence by owning and optimizing Clinical Supply Chain processes, influencing change, and ensuring global system integration.
• Collaborate with Technical Development Teams and Clinical Operations to bridge the gap between drug development and patient-centric delivery.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level