Director – Supply Chain

Director – Supply Chain

Requirements

• 12+ years of relevant experience in related field and a BS or BA; OR
• 10+ years of relevant experience and a MA/MBA OR
• 8+ years of relevant experience and a PhD

Responsibilities

• Serves as the clinical supply lead on PDM sub-teams especially for complex development programs – e.g., late phase, acquisition, partnership/alliance, new modality, etc.
• Leads the development and execution of overall clinical supply strategy and management for clinical development program(s), including management of investigational medicinal product (IMP) for assigned global trials.
• Often in a matrix environment, oversees and supports clinical study planners. Facilitates issue and risk identification, mitigation, resolution and communication.
• Drives decision-making at cross-functional teams (ClinOps, PDM sub-teams) supporting the long-term vision.
• Identifies, manages and mitigates supply risks at clinical development program level. Leads and drives visible, impactful process improvements, change business and organizational imperatives.
• Authors, revises and reviews standard operating procedures (SOPs), work instructions and business policies.
• Accountable for clinical supply budget of assigned clinical development program(s).
• Reviews and approves statement of work, purchase orders and invoices.
• Influences, at times drives, program allocations at partners, contract manufacturing organizations (CMOs).
• Lead or a contributing member to GCSC, GSC or PDM strategic initiatives including and not limited to due diligence resource pool, global drug delivery community, clinical supply integration due to M&A and policy topic member supporting the External Advocacy Steering Team (EAST).

Preferred Qualifications

No preferred qualifications provided.