Supply Chain Study Manager
Dfind Science & Engineering AB / Apotekarjobb / Göteborg
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Supply Chain Study Manager at AstraZeneca
We are now looking for a Supply Chain Study Manager for a consultant assignment during 2017 at AstraZeneca
Employer: Dfind Science & Engineering
City: Göteborg
Extent: Full time
The Arena
As a Supply Chain Study Manager in Supply Chain/Pharm Dev, you'll 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. We'll look to you to design, plan and manage trial medication for patients taking part in AstraZeneca clinical studies all over the world. In return, you'll find a vibrant team culture in which continuous improvement and effective collaboration are high priorities.
The Role
The Supply Chain Study Manager (SCSM) role is a key leadership role within R&D Supply Chain. The role holder will manage the supply chain for a portfolio of global clinical studies across all phases within a drug development programme. He / she will lead cross-functional Study Drug Working Group (SDWG) and represent these teams on the R&D Supply Chain Team. The SCSM works in collaboration with customer functions to influence and manage demand for individual studies, and is responsible for their supply chain deliverables.
The Supply Chain Study Manager role covers the full spectrum of the clinical study lifespan, across all phases of the drug development lifecycle, covering small and large molecule drug products.
Within this role the SCSM will collaborate with members of R&D SC, Clinical Development and external partners.
Within this role the SCSM will:
• Lead and provide direction to Study Drug Working Groups (SDWGs) comprising members of R&D SC, 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.
• Understand and translate clinical study protocol requirements into demand for drug product within a clinical study. Author the drug supply section of Clinical Study Protocol and lead development of master label text.
• 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. Define IVRS user requirements, set up IVRS tool and ensure timely go-live for individual studies. Use IVRS to track recruitment and adjust IVRS parameters to accommodate any changes in study scope and design.
• 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. Flag deviations to SC Programme Manager. 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.
Preferred experience/requirements
The ideal candidate for this role will have an R&D background and strong ability to manage their time effectively, working on several studies or tasks within studies alongside each other and prioritizing between them as needed. They will thrive in a fast paced role where there is often change to the studies, using effective evaluation and analysis of complex data sets to make decisions throughout the life of the studies. They will manage business and supplier relationships well and be able to influence others cross functionally and globally.
Minimum experience
• A suitable degree, qualification or experience in a supply chain drug development discipline. e.g. Pharmacist.
• Experience in managing and influencing customer demands.
• In depth knowledge of Clinical Development processes relevant to the supply of clinical materials.
• Experience of project management.
• Strong influencing, negotiating and problem-solving skills, including across functional, geographical and cultural boundaries.
• Risk identification and management.
• Excellent written and verbal communication skills in Swedish and English.
Last date of application: 2016-11-10 but we are interviewing applicants continuously, so please send your application as soon as possible.
For information: Eleonor Ehrman 073-3434109 or Birgitta Nyström 073-3434153
Organisations-/företagsbeskrivning:
Dfind Science & Engineering är ett konsult- och rekryteringsföretag specialiserade på kompetenser inom naturvetenskap och teknik. Med engagemang och lyhördhet hjälper vi människor och företag att hitta lösningar för att utvecklas. Hos oss har du möjlighet att utveckla dina kunskaper och färdigheter genom uppdrag hos våra utvecklings- forsknings- och produktionsintensiva kunder i Norden.
Vi tycker att det är viktigt att all kompetens på arbetsmarknaden tillvaratas. Vi välkomnar alla sökande och eftersträvar mångfald. Dfind Science & Engineering ett auktoriserat bemanningsföretag via Almega och följer deras kollektivavtal.
Varaktighet, arbetstid
Heltid Tillsvidare
Publiceringsdatum2016-11-01ErsättningFast lön
Så ansöker duSista dag att ansöka är 2016-11-12
Ange följande referens när du ansöker: 200997733
Klicka på denna länk för att göra din ansökanKontaktEleonor Ehrman
eleonor.ehrman@dfind.seFöretagDfind Science & Engineering AB
AdressDfind Science & Engineering AB
Östra Hamngatan 23
41110 GÖTEBORG
KontorsadressÖstra Hamngatan 23, 41110 GÖTEBORG
Jobbnummer 3139444
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