Supply Chain Study Manager to AstraZeneca
Proffice Life Science AB / Apotekarjobb / Mölndal
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hela Sverige We are now recruiting a Supply Chain Study Manager for an assignment at Supply Chain Management at AstraZeneca Mölndal. Preferred starting date is 1 December, and the position duration is 11 months.
The Supply Chain Management (R&D SCM) department in Mölndal is a part of the global Pharmaceutical Development organization of AstraZeneca. There are 50 Supply Chain Study Managers working globally in US, UK and Sweden. They design, plan and manage trial medication for patients taking part in every AstraZeneca clinical study all over the world.
As a Supply Chain Study Management (SCSM) you will manage the supply chain of investigational products for a portfolio of global clinical studies across all phases within a drug development programme. The role holder will lead the Study Drug Working Group - SDWG responsible for the logistics of the study drug. This team comprises members of R&D Supply Chain, Clinical Development and external partners. The Supply Chain Study Manager will ensure that the teams operate within set boundaries, so that the clinical supplies are delivered effectively and consistently, balancing cost and risk.
In your daily work you will be expected to translate clinical study protocol requirements into demand for drug product, including requirements for placebo, comparators and rescue/challenge medication. You will also be expected to manage Interactive Voice/Web System (IV/WRS) for your studies. This will include defining user requirements, set up IV/WRS tool, ensure timely go-live for individual studies and to use IV/WRS to track recruitment and adjust IV/WRS parameters during the study.
The Supply Chain Study Management will collaborate with CRO partners in different functions (e.g. for pack designs, IV/WRS delivery or Clinical Operations), and will review the technical part of the outsourcing contract.
We are looking for a person with an MSc degree (or equivalent) in subjects related to supply chain or drug development disciplines. The position requires in depth knowledge of Clinical Development processes relevant to the supply of clinical materials, and documented experience of project management. Experience of IV/WRS and set-ups is advantageous as well as experience managing CRO-contacts and influencing customer demands.
To be successful in this role it is essential to have excellent communication and social skills as well as being a strong problem solver. Candidates should be able to work independently, take own initiatives and have a positive goal oriented attitude. Good collaborative skills are necessary and you should be comfortable to work in an international environment. Excellent English and Swedish is required, both spoken and in writing.
We are continuously interviewing candidates since we are aiming at filling the position as soon as possible. For further information, please contact Klara Thorsson 0733-434777 or Ulrica Marklund 0733-434446
Publiceringsdatum2011-11-04Arbetstider och omfattningTillsvidare
Heltid
ErsättningFast lön
Så ansöker duSista dag att ansöka är 2011-11-06
Please apply in English at
www.proffice.se/lifescienceAnsökan kan tyvärr inte göras via e-post.
FöretagPROFFICE LIFE SCIENCE AB
AdressPROFFICE LIFE SCIENCE AB
BOX 70368
10724 STOCKHOLM
KontorsadressMÄSTER SAMUELSGATAN 60
STOCKHOLM
KontaktuppgifterTelefonnummer: 08-7871700
Jobbnummer 1072097
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