AddressRole Name: Clinical Study Supply Lead
Location: Macclesfield- UK
Competitive Benefits & Salary
Make a positive impact, in a team where it means more
In Operations, we have a big ambition – to deliver more medicines to patients, quicker and more affordably. Backed by the investment, leadership, and a clear plan to get there, we bring personal dedication and out of the box thinking.
We are driven by our dedication to deliver accelerated growth for AstraZeneca and to make people’s lives better. It pushes us to keep building on our foundations and progressing as we turn our ever-growing and increasingly sophisticated pipeline from molecule to medicine. Be part of evolving how we work with Lean, ground breaking science, digitalisation and balanced practices.
We have exciting opportunities for Clinical Study Supply Leads (CSSLs) to join our team! The CSSL is a key role within our Clinical Manufacturing and Supply teams. Based at our Macclesfield site, this role involves planning and project managing a portfolio of studies across all phases of a drug development programme ensuring on time delivery to patients.
This position is placed within Pharmaceutical Technology and Development (PT&D), the bridge that turns brilliant science into actual medicines that help millions of people.
The CSSL plans and executes supply chain for one or more global clinical studies across all phases within drug development. The CSSL holds overall accountability for delivery of Intellectual Property and co-ordinates associated tasks and activities across all relevant functions within the supply chain. The Role will have multiple contacts across internal and external groups including leadership of working groups.
What you'll do
Plan and Project manage the packaging, labelling and delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply, following defined business processes
Lead the Study Drug Working Group and contribute to the Supply Chain Team Meetings enabling continuous cross-functional dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study
Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls
Understand customer demand requirements and have the ability to forecast and translate this into a supply plan
Manage the Interactive Response Technology (IRT) system to execute demand and supply planning
Take ownership for Inventory management, utilising systems such as Smart Supplies, including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction, supporting waste reduction.
Ensure effective communication with project teams and key partners across a global network
Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies, ensuring consistent on time delivery of drug to patient
Supervise the budget for your individual study supply activities and materials for the project including packaging, labelling and distribution costs
Required Skills & Knowledge
Bachelor’s degree in a scientific or business subject area – equivalent experience will be considered
Experience within a supply chain environment or pharmaceutical industry
Holistic knowledge of end to end supply chain activities with proven track record of successful demand and supply planning
Experience in running projects and influencing customer demands
Analytical aptitude, showing strong data analysis skill base and ability to utilise dashboards
Strong influencing, negotiating and problem-solving skills, across geographical and cultural boundaries
Risk identification and management
LEAN capabilities
Proficient IT skills with an ability to adapt and operate in specific multiple systems
Desirable Skills & Knowledge
Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice)
Knowledge of clinical development processes relevant to the supply of clinical materials
Experienced in handling Quality Events (Deviations, Change Controls, Complaints)
Use of either Smart-Supplies or other sophisticated planning tools and applications would be an advantage
At AstraZeneca, we 're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and fuel your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth and development.
So what's next?
Apply today! Please include your CV and a Cover Letter in your application.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
