Supply Chain Study Managers to AstraZeneca, Gothenburg!
Modis Sweden AB / Läkarjobb / Göteborg
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hela Sverige MODIS Life Science is looking for 2 Supply Chain Study Managers to AstraZeneca, Gothenburg. It is preffered that you have a pharmaceutical background with deep knowledge of the Clinical development processes and project management skills.
The consultant assignment will start May 1st and proceed until 2019-08-31
Welcome with your application no later than March 28th
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.
About Modis
We are constantly striving to support our customers and consultants to become successful. As a consultant, you are our top priority and when you need us, we will be there for you.
We will include you in our business and to our customers. You are our most important asset and for us to stay ahead you will take an active part in our business development and our offers to the market.
By becoming our colleague, your daily life as a consultant will be shifting with different assignments and projects in a variety of industries, systems and environments. Your experience will increase as well as your social and professional network. As a consultant, you are covered by collective agreements, insurance, occupational healthcare, healthcare and discounts on training cards. We believe in connecting people so having regularly social activities is key for us.
Modis delivers a wide range of services and competencies within IT, Engineering and Life Science. Our services are characterized by speed, simplicity and quality. Modis is represented in the United States, Canada, Europe with over 100 offices and with more than 35,000 colleagues on assignments each day.
Varaktighet, arbetstid
Heltid Visstid
Publiceringsdatum2018-03-14ErsättningFast lön
Så ansöker duSista dag att ansöka är 2018-03-29
Klicka på denna länk för att göra din ansökanKontaktNalin Yilmaz
Nalin.Yilmaz@modis.seFöretagModis Sweden AB
AdressModis Sweden AB
Postgatan 28
41110 Göteborg
KontorsadressPostgatan 28
Jobbnummer 4020261
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