Clinical Study Administrator at AstraZeneca Gothenburg
Dfind Science & Engineering AB / Apotekarjobb / Göteborg
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At AstraZeneca they work together across global boundaries to make an impact and find answers to challenges. They do this with integrity, even in the most difficult situations because they are committed to doing the right thing.
This is an exciting period for them, as well as for those poised to join them. Their strategy and ability to transform their portfolio means they 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
Business: Dfind Science & Engineering
City: Gothenburg
Deadline for applications: 2019-04-16. Selection is on-going and interviews will be held continuously which means the position can be filled before deadline. Please make sure to send in your application at your earliest convenience!
For more information contact: Malin Wåhlberg
malin.wahlberg@dfind.se or Birgitta Nyström
birgitta.nystrom@dfind.sePlease keep in mind, e-mail applications will not be considered. Register your profile at Dfind Science & Engineering's webpage and send in your application there.
Organization/Business description:
Dfind Science & Engineering is a recruitment and consulting company within science and engineering. All our consultant managers and recruitment consultants have an education and work experience within the respective field. In combination with extensive knowledge of staff issues and solid experience of recruitment, this means that we understand our clients' need for both flexibility and the right skills.
Dfind Science & Engineering is since 2016 part of Randstad Group. With over 600 000 employees in over 40 countries Randstad is the world's largest company within recruiting and staffing.
Varaktighet, arbetstid
Heltid Tillsvidare
Publiceringsdatum2019-04-10ErsättningFast lön
Så ansöker duSista dag att ansöka är 2019-04-20
Ange följande referens när du ansöker: 201214501
Klicka på denna länk för att göra din ansökanKontaktBirgitta Nyström
birgitta.nystrom@dfind.seFöretagDfind Science & Engineering AB
AdressDfind Science & Engineering AB
Södra Hamngatan 35
41114 GÖTEBORG
KontorsadressSödra Hamngatan 35, 41114 GÖTEBORG
Jobbnummer 4726291
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