Supply Chain Study Managers
Alten Sverige AB / Sjukhusteknikerjobb / Göteborg
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hela Sverige ALTEN Pharma is looking for two
SUPPLY CHAIN STUDY MANAGERS for consultancy assignments at AstraZeneca in Gothenburg.
THE ARENA
As a Supply Chain Study Manager in Supply Chain/Pharm Dev, you will develop a broad knowledge of the diverse range of clinical study options utilized by the pharmaceutical industry, as well as in-depth expertise in specific therapeutic areas. We will 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 will 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 ALTEN
For over 20 years, ALTEN has developed its business by keeping to the core values ??that have built up the company's success. Every year, hundreds of ALTEN consultants have been given the opportunity to embark on challenging technical projects for our customers. ALTEN has a tradition of developing products in many areas, and history in Sweden is based primarily on skills in mechanics, software and electronics. Thanks to a successful concept in which we utilize the expertise of experienced consultants and develop young abilities towards a successful career, we have gained ground in many industries. Our Pharma initiative is based on the same successful concept with the same strong structure, but in a new exciting industry and a new field of expertise that includes knowledge in chemistry, biotechnology and biomedicine.
As an employee at ALTEN, we offer you a competitive salary based on your performance and work experience. You also have the opportunity to influence your assignments, different benefits and your overall working environment as well as choose your career path. We offer a wide range of internal trainings and an opportunity to plan for an international career. It is our conviction that genuine commitment is created through choice and the ability to influence your own personal development - our business model provides that opportunity. This freedom of choice enables us to offer our clients the most committed consultants, regardless of assignments. At ALTEN, we believe in growing together!
For questions about the position, please contact Nils Löfgren, Business Manager Pharma, at
nils.lofgren@alten.se.
Varaktighet, arbetstid
Heltid Tillsvidareanställning
Publiceringsdatum2018-03-14ErsättningEnligt överenskommelse
Så ansöker duSista dag att ansöka är 2018-03-28
Klicka på denna länk för att göra din ansökanKontaktHR-avdelningen, Alten
FöretagAlten Sverige AB
AdressAlten Sverige AB
Theres Svenssons gata 15
41755 Göteborg
KontorsadressTheres Svenssons gata 15, Göteborg
Jobbnummer 4020328
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