
Manager, Clinical Supply
BlueRock Therapeutics
full-time
Posted on:
Location Type: Hybrid
Location: Toronto • Canada
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Salary
💰 CA$130,000 - CA$155,000 per year
About the role
- Own CSI hub scheduling and forecast alignment based on trial enrollment and treatment center surgical capacity
- Lead the monthly rolling forecast process with Clinical Operations, including demand/supply reconciliation, assumptions, constraints, and action planning
- Partner with Clinical Ops to translate enrollment updates, protocol changes, and planning scenarios into hub plans and supply readiness actions
- Serve as PM and lead facilitator for the Clinical Supply Integrated Planning (CSIP) forum, including agenda setting, pre-reads, decision capture, action tracking, and risk escalation
- Lead cross-functional planning standups across Supply Chain to ensure readiness, alignment on constraints, and clear inter-functional commitments
- Represent Tech Ops / Clinical Supply as the primary planning interface in Clinical Operations meetings and program forums
- Build, maintain, and improve integrated planning dashboards, KPIs, and leadership reporting
- Lead scenario planning and tradeoff analysis, and provide recommendations to support leadership decision-making
- Consolidate clinical and non-clinical CSI hub demand, including engineering runs, tech transfer, and training activities, into one integrated planning view
- Standardize and continuously improve integrated planning processes, governance, and documentation, while supporting scalable operating models and providing backup coverage for critical logistics operations as needed
Requirements
- Bachelor’s degree in Supply Chain, Engineering, Life Sciences, Business, or related field
- Manager: 11+ years of experience in clinical supply, manufacturing operations, supply chain planning, integrated planning, or program management within biopharma/pharma
- Demonstrated experience translating clinical demand signals into operational plans across manufacturing networks (internal and/or external/CDMO)
- Strong program management skills (governance, stakeholder alignment, action/risk management, executive communication)
- Strong analytical capability: KPI definition, dashboarding, and data storytelling for decision-making
- Experience operating in regulated environments and familiarity with GxP expectations and documentation discipline
- Proficiency with planning and reporting tools (e.g., Excel, Smartsheet) preferred; ERP familiarity such as SAP/Oracle a plus)
- Excellent communication and facilitation skills; ability to lead without authority and drive alignment across competing priorities
- Compare clinical trial portfolios and apply phase appropriate planning standards and proactively surface conflict, tradeoffs and recommendations
- This role is a hybrid role based out of Toronto
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
supply chain planningintegrated planningprogram managementanalytical capabilityKPI definitiondata storytellingscenario planningtradeoff analysisdemand/supply reconciliationrisk management
Soft Skills
communicationfacilitationleadershipstakeholder alignmentaction trackingdecision capturegovernanceexecutive communicationproblem-solvingcollaboration