Supply Chain Study Manager (scsm), Mölndal
Experis Engineering Huvudkontor / Företagsförsäljarjobb / Mölndal
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Experis Engineering offers specialists and managers through interim consulting, recruitment and project solutions. By combining our industry experience with our knowledge of human potential, we make both individuals and businesses grow and develop.
Experis Engineering is present on 30 locations in Sweden and in more than 50 countries worldwide.
The role
The Supply Chain Study Manager (SCSM) role is a key 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.
The SCSM works in collaboration with customer functions to influence and manage demand for individual studies, and is responsible for their supply chain deliverables through leadership of the Study Drug Delivery Team.
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 cGMP Quality Management Systems, including managing deviations, complaints, change controls as appropriate.
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.
Contact/Application
If you are the person we are looking for you are welcome to apply for this job through the link on this site.
The selection process will be short so please send in your application as soon as possible with CV and personal letter written in English.
Do not hesitate to contact Caroline Lindberg Sen, at Experis Engineering, for further questions:
caroline.lindberg.sen@se.experis.comPubliceringsdatum2014-11-26Arbetstider och omfattning100% Enligt överenskommelse
ErsättningEnligt överenskommelse
Så ansöker duSista dag att ansöka är 2014-12-08
Klicka på denna länk för att göra din ansökanKontaktCaroline Sen
FöretagExperis Engineering Huvudkontor
AdressExperis Engineering Huvudkontor
Klarabergsgatan 29
11181 Stockholm
KontorsadressKlarabergsgatan 29
Jobbnummer 2082231
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