Clinical Study Administrator at AstraZeneca
Modis Sweden AB / Övriga jobb / Göteborg
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hela Sverige Modis Life Science is now looking for a Clinical Study Administrator to AstraZeneca in Gothenburg. This is a consultancy assignment initially for 6 months. As a consultant you will employed at Modis and work on the assignment at AstraZeneca. If you find the role interesting, send your CV (in English) and application no later than April 16th.
About the company
At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with integrity, even in the most difficult situations because we are committed to doing the right thing.
This is an exciting period for us, as well as for those poised to join us. Our strategy and ability to transform our portfolio means we have a late stage pipeline that presents incredible opportunities to push the boundaries of science to deliver life-changing medicines.
As a Clinical Study Administrator, you will be accountable for assisting the Associate Director Study Management (ADSM) and the (Senior) Study Management Associate(s) to fulfil their accountabilities through coordinating activities that ensure quality and consistency and providing administrative support. You can also be responsible for keeping systems updated in studies with external partners.
You will work across several clinical studies. The exact accountabilities will differ depending on the exact nature of the clinical programme, so you 'll need a high degree of flexibility.
Role duties & responsibilities
• Collect, review and track clinical documents, as required by the study
• Ensure that all relevant Study documents are uploaded to Veeva Vault, our eTMF system, in a timely manner
• Support production of study documents, ensuring template and version compliance
• Set-up, populate and accurately maintain information in AstraZeneca tracking and communication tools
• Manage and contribute to coordination and tracking of study materials and equipment
• Coordinate tasks during the study process, audits and regulatory inspections.
• Lead the practical arrangements, contribute to the preparation of internal and external meetings e.g. study team meetings, monitor meetings, Investigator meetings. Liaise with participants and/or vendor
• Contribute to and distribute presentation material for meetings, newsletters and web-site.
Skills & Experience
• Basic understanding of the drug development process.
• Basic knowledge of ICH-GCP principles
• Ability to manage multiple deliverables
• Experience in operational support in clinical development would be desirable
For questions, please contact Cecilia Larzon (
cecilia.larzon@modis.se)
Varaktighet, arbetstid
Heltid Tillsvidare
Publiceringsdatum2019-04-11ErsättningFast lön
Så ansöker duSista dag att ansöka är 2019-04-17
Klicka på denna länk för att göra din ansökanKontaktCecilia Larzon
FöretagModis Sweden AB
AdressModis Sweden AB
Postgatan 28
41110 Göteborg
KontorsadressPostgatan 28
Jobbnummer 4725921
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