Supply Chain Study Manager, AstraZeneca Gothenburg
Adecco Sweden AB / Övriga jobb / Mölndal
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hela Sverige Do you have an R&D background with project management experience and knowledge about the supply chain drug development? An exciting opening is now available as a Supply Chain Study Manager at AstraZeneca, Gothenburg. You should be able to manage your time effectively since the role includes coordinating several studies and prioritizing between them.
This is a temporary position as a consultant for 1 year, planned to start January 2017 or as soon as possible. Last day to apply is November 14, but interviews are held continuously so send your application as soon as possible.
The Role
The Supply Chain Study Manager (SCSM) role is a key role within R&D Supply Chain. The role holder will manage and coordinate the drug 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 members of R&D SC, Clinical Development and external partners to manage drug demand for individual studies and is responsible for the drug supply deliverables.
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. 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, coordinating several studies or tasks within studies alongside each other and prioritizing between them as needed. He/she 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.
* 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.
What do we offer?
Adecco Life Science is a specialized Business Line within Adecco. We work exclusively with Staffing Services and Recruitment of personnel within the Life Science industry. Our expertise lies within all areas of Life Science such as R&D, Production, Quality Assurance, Clinical Research, Regulatory Affairs, Medical Affairs, Marketing & Sales and many more. Our customers are companies, of different sizes, within the Pharmaceutical-, Biotech- and Medtech- industries. As the largest recruiting and staffing company in the world our most valuable assets are our consultants. With us, you as a consultant will be appreciated for your difference-making competence within Life Science!
Adecco Life Science can offer you the opportunity of interesting assignments and positions at attractive companies that perhaps never will be put out on the open market! For your security as a consultant, you are covered by our collective agreement and by insurance and corporate healthcare. We also want you to stay healthy and therefore offer you healthcare contributions and discounts on training cards. We arrange social activities continuously where you are able to share your experiences with our other consultants.
Are you interested?
Then you should apply as soon as possible. The position is soon to be filled and therefore work with recruitment is being done on a continual basis.
Unfortunately we can not accept applications through e-mail, but if you have questions regarding the position contact Nalin Yilmaz,
nalin.yilmaz@adecco.se.
We look forward to your application!
Varaktighet, arbetstid
Heltid Visstid
Publiceringsdatum2016-11-11ErsättningFast lön
Så ansöker duSista dag att ansöka är 2016-11-14
Klicka på denna länk för att göra din ansökanKontaktNalin Yilmaz
nalin.yilmaz@adecco.seFöretagAdecco Sweden AB
AdressAdecco Sweden AB
Kungsgatan 60
10224 STOCKHOLM
KontorsadressKungsgatan 60
Jobbnummer 3155448
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