# Senior Director, Clinical Study & Supply Planning at AstraZeneca

AI Level 1, AI centrality 0 out of 100. Poland - Warsaw.

## Details

- Company: [AstraZeneca](https://jobsbylevel.com/companies/astrazeneca)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Poland - Warsaw
- Posted: October 7, 2026
- Apply: https://jobsbylevel.com/go/5a134f7c-c197-4f54-a82d-df376ca7a626

## Description

Title: Senior Director, Clinical Study & Supply Planning Location: Warsaw Model: hybrid 3+2 Job Description As the Senior Director – Study & Supply Planning, you will lead a global, multi-layered organisation accountable for the end-to-end supply planning and study execution of clinical supply across AstraZeneca’s development portfolio within Clinical Supply & Manufacturing Organisation (CM&S). You will be responsible for ensuring the seamless integration of programme-level supply planning and study-level lifecycle management, enabling reliable, compliant, and efficient delivery of investigational products to patients in the [Oncology / Biopharma] portfolio, working closely across CM&S to align supply planning and execution with the rest of the organisation. You and your teams will partner with senior leaders across Clinical, CMC, Quality, Regulatory, and external partners to ensure aligned delivery of clinical trials, proactively managing risk and ensuring no interruption to patient supply. You will drive enterprise-level performance, embed standardisation and continuous improvement, and develop future-ready capabilities to support AstraZeneca’s pipeline. Core Accountabilities Defines and delivers the integrated strategy for Clinical Study & Supply Planning, ensuring alignment with R&D priorities and AstraZeneca’s enterprise objectives In conjunction with the [Oncology / Biopharma] Snr Dir Study & Supply Planning, owns and evolves the operating model across Supply Planning, and Study Lifecycle Management, ensuring clarity of roles, decision rights, and escalation pathways Ensures delivery of constrained, optimised supply plans across all BOM levels (API → DP → primary and secondary kits), balancing service, cost, risk, and plan stability Oversees programme-level supply planning, including scenario development, inventory strategy, allocation decisions, and order release across the supply chain Ensures excellence in study-level lifecycle management, overseeing end-to-end study lifecycle delivery including setup, change management, and closure Drives effective management of study risks, issue resolution, and customer service impacts (including FSI & OOD), ensuring timely escalation and resolution Leads portfolio-level performance, ensuring on-time in-full delivery of clinical supplies, study milestone adherence, and predictable execution Oversees critical supply decisions including inventory optimisation, rework strategies, and shelf-life extensions, ensuring supply continuity and minimisation of waste Ensures full compliance with GMP, GCP, and regulatory requirements, maintaining inspection readiness and robust management of quality events Collaborates with senior stakeholders across Clinical Operations, CMC, Supply Chain, Regulatory and Quality to enable aligned, cross-functional decision making Drives continuous improvement and standardisation of processes, tools, and performance management frameworks across planning and execution Champions a culture of innovation, digital enablement, and operational excellence to support future pipeline needs Leads organisational capability development, ensuring strong talent pipelines, succession planning, and leadership capability Manages organisational resource levels in line with budget & drive annual productivity and strategic improvement Essential Bachelor’s degree in Supply Chain, Life Sciences, Engineering, or related discipline Extensive leadership experience (10+ years) in (clinical) supply chain, planning, or clinical operations Proven experience leading large, complex, global organisations, including leading leaders Deep expertise in: (Clinical) supply planning (constrained planning, inventory management, S&OP) Clinical study execution and lifecycle delivery Strong knowledge of drug development processes and GxP regulatory requirements (GMP/GCP) Demonstrated ability to operate at portfolio and enterprise level, balancing strategy and delivery Proven ability to drive

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