Senior Clinical Supply Study Lead

Tryzenoya

Design and execute optimized supply chains
Delivery of ip to a specific study
Planning best practice
The Senior Clinical Supply Study Lead designs and executes optimized supply chains for complex global clinical studies across all phases within drug development

Job Summary

  • The Senior Clinical Supply Study Lead designs and executes optimized supply chains for complex global clinical studies across all phases within drug development.
  • Key responsibilities include study delivery execution, mentoring experienced colleagues, leading business development projects, and driving improvements in supply chain excellence and digital capability.
  • The role involves influencing study design, managing stakeholders, overseeing demand and supply planning, cost management, and ensuring compliance with GMP & GCP standards.

Matching Summary

The Senior Clinical Supply Study Lead designs and executes optimized supply chains for complex global clinical studies across all phases within drug development.

Skills & Requirements

Must-have

  • design and execute optimized supply chains
  • delivery of IP to a specific study
  • planning best practice
  • supply planning systems proficiency
  • leadership of working groups
  • drive improvements and processes
  • supply chain excellence
  • digital capability implementation
  • business process owner
  • risk identification and mitigation
  • Lean Leadership Habits and Behaviours
  • Study Design influence
  • Stakeholder management
  • Supply Chain Team Meetings collaboration
  • Kick Off Meetings for suppliers
  • escalation of risks/issues/concerns
  • outsourced studies support
  • knowledge sharing among peers
  • Demand and Supply planning
  • study demand forecasting
  • secondary packing supply plan
  • change management execution
  • inventory management
  • waste reduction
  • cost management
  • packaging, labelling and distribution costs
  • AQI RE process
  • study spend control
  • budget constraint flagging
  • Quality Events management
  • GMP & GCP audits contribution
  • TIER meetings updates
  • eTMF compliance
  • OOD reporting
  • IRT Smart Supplies platform utilization
  • N-Side Suite utilization
  • Packing/labelling/distribution activities definition
  • PLD strategy definition
  • Kit/Pack design
  • TCM implementation
  • Master Label development
  • Destruction management
  • Expiry date management
  • Extension of shelf life
  • Rework & recalls management

Nice-to-have

  • mentoring and support to colleagues
  • driving improvements and processes
  • business development projects contribution
  • collaboration with Dev QA, Analytical, CMC, SCPL & Clinical partners
  • partnership with CSOS colleagues
  • creating great place to work environment

Key Requirements

  • Supply chain and drug development process knowledge
  • Awareness of GXP Standards
  • Demand planning and forecasting experience
  • Proven track record of optimized demand and supply planning in Phase III studies
  • Experience of managing projects
  • Proficient IT skills
  • Strong influencing, negotiating and problem solving skills
  • Working knowledge of Clinical Trial Directive
  • Knowledge of Clinical Development processes
  • Lean experience/qualifications
  • >2 years’ CSSL experience

Work Rights

Not specified

Tailored Resume

Cover Letter