Clinical Study Supply Lead
AstraZeneca AB / Administratörsjobb / Göteborg
2019-12-03
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Do you enjoy new challenges and have leadership skills? Are you interested to take your skills and experience to a new level in the pharmaceutical industry? We are looking for a Clinical Study Supply Lead to join our Clinical Study Supply Chain team in Gothenburg - so here is your opportunity!
As a Clinical Study Supply Lead you will:
* Be part of the Global Clinical Supply Chain organisation.
* Lead a cross functional team that delivering supply to clinical studies across the world.
* Design, plan and manage trial medication for patients taking part in AstraZeneca clinical studies.
* Develop a broad knowledge of the diverse range of clinical study options utilised by the pharmaceutical industry, as well as in-depth expertise in specific therapeutic areas.
*
Work closely with both internal and external suppliers.
In return, you will find and play a part of a vibrant team culture in which continuous improvement and effective collaboration are high priorities.
Your Main Responsibilities as CSSL:
* Lead and provide direction to Study Drug Working Groups, consisting of members of Clinical Manufacturing and Supply, Clinical Development and external partners.
* Ensures the team delivers clinical supplies effectively and consistently, balancing cost and risk to supply with expert input and support from cross functional groups.
* Use simulation tools and supply chain expertise to design optimised, lean supply chains for individual studies and ensure delivery of the end to end supply of materials to meet study needs.
* Collaborate with CRO partners in development of pack design and review the technical part of the outsourcing contract. Review changes to the contract with CRO partners and Sourcing Managers as necessary.
* Monitor the budget for individual study supply activities and materials for the project. Manage change in demand and supply, resolve issues, escalating when appropriate.
* Work within GMP Quality Management Systems, including managing deviations, complaints, change controls as appropriate.
Essential Requirements
We believe you have:
* Relevant Academic degree - e.g. BSc/MSc in Clinical Pharmacy
* Great knowledge of Clinical Supply to be able to understand and translate clinical study protocol requirements into demand for drug product within a clinical study.
* Acquaintance to author the drug supply section of Clinical Study Protocol and lead development of master label text.
* Knowledge to define IRT user requirements and use IRT to track recruitment and adjust IRT parameters to accommodate any changes in study scope and design.
* Experience in drug development discipline. e.g. Pharmacist
* Experience from a manufacturing organization or previous working knowledge of Lean
* Documented strong leadership and change management capabilities
* Willingness to drive change in the Supply Chain activities in a manufacturing environment
* Excellent communication skills in both Swedish and English, both verbally and in writing
* Knowledge of Clinical Development processes relevant to the supply of clinical materials
* Strong influencing, negotiating and problem-solving skills, including across functional, geographical and cultural boundaries
If you are interested - welcome with your application today!
AstraZeneca is acting as an Employment Agency in relation to this vacancy.
Varaktighet, arbetstid
Heltid Permanent
Publiceringsdatum2019-12-03ErsättningNot Specified
Så ansöker duSista dag att ansöka är 2019-12-13
Klicka på denna länk för att göra din ansökanFöretagAstrazeneca AB
Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "R-064347".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Astrazeneca AB (org.nr 556011-7482)
Arbetsplats AstraZeneca
Jobbnummer 4985073
Observera att sista ansökningsdag har passerat.