Clinical Supply Director

As a Clinical Supply Director, you will play a critical role within Clinical Manufacturing & Supply, owning the end-to-end clinical supply chains for a global programme of products. You will oversee the full lifecycle of clinical programmes-across all phases of drug development-and support both small-molecule and large-molecule portfolios.
In this role, you will be accountable for shaping and executing the long-term strategy for one or several complex, high-profile clinical supply chains. You will act as a key influencer in the design of these supply chains, ensuring they are robust, efficient, and aligned with programme needs.
You will work across multiple organisations and functions, representing R&D Supply Chain at PT&D and Global Project Teams. You will lead matrixed, multi-functional international teams, driving strategy, embedding best practices, and managing supply chain performance through critical KPIs.In addition, you will serve as a Business Process Owner for key processes or drive the development of new business processes and ways of working to enhance overall supply chain effectiveness.
Your New Role
Accountable for the development, long-term strategy and performance of clinical supply chains, owning the E2E supply of products in the development portfolio.Influential in the design phase with relevant experts to drive optimised design with respect to quality, risk and cost for the businessLeads the Supply Chain Team (SCT) which is accountable for developing and maintaining the supply plan for the project. Work in conjunction with the Supply Chain Planner to guarantee: Balancing Short to Mid-term Supply and Demand, Inventory Management, input into D&OP Process, Planning Excellence Process Requirements, Master Data ManagementOverall endorsement of the supply plan is the Sr CSPL accountabilityMonitors the performance of the supply chain and optimise for higher volume phases of the project, balancing speed, quality and cost with respect to the agreed level of risk.Accountable for a significant budget for supply activities and materials for the project.Manages change in demand and supply,
resolve issues, escalating when appropriate.Maintains appropriate information for supply activities in PLANIT on an ongoing basis and in line with RBU.Ensure ongoing supply through transition from development sources to commercial sources of manufacture.Understands and acts according to GxP and knows the impact it has on supply chain activities.Ensure timely delivery of information to meet internal and external regulatory and legal requirements.Take responsibility for managing issues and making complex trade-offs with both internal and external stakeholders. This will require well developed conceptual and analytical thinking to make complex judgements and deliver innovative solutions.Take a lead in motivating/mentoring others within the function and continually develop competence.Business Process Owners for key processes; developing, improving and promoting lean and supply chain practices within and across interfacing functionsBe responsible for introducing innovation into the Supply
chain ensuring a culture of continuous improvement is encouraged and managed.Act as a sponsor to support and manage the implementation of supply chain change and be the 1st point of contract for Senior Stakeholders within the organizations regarding your portfolio of products
Essential Skills
In depth knowledge of supply chains and drug development process.In depth knowledge of Clinical Development processes relevant to investigational products.Awareness of GXP Standards within a Clinical environmentDemand management and forecasting experienceIn depth experience of project management, influencing and managing business partner relationshipsProficcient IT skills with an ability to adapt and operate in multiple systemsStrong influencing, negotiating and problem solving skills across geographical and cultural boundariesEducation acc. to CV. Bachelor Degree (equivalent) or higher
Desirable Skills
Working knowledge of the Clinical Trial Directive and global regulatory environment impacting the provision of investigational products
WHY ASTRAZENECA?
It's an exciting time to join AstraZeneca, a global business that's rapidly growing - there's a lot happening and even more to come. And we are a valued part of this journey. Respected partners across the business, we provide the platform that's going to power us to achieve more.
So, what's next?
Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available, and we hope it's yours. Please apply with a copy of your CV.