Clinical Study Administrator to Astra Zeneca
Adecco Sweden AB / Administratörsjobb / Mölndal
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hela Sverige AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
To Study Operations in Early Clinical Development, IMED, we are looking for a Clinical Study Administrator for a 6 months period.
The Arena:
Early Clinical Development is a dedicated clinical scientific resource for AstraZeneca 's early development portfolio, which provides a translational medicine capability to rapidly understand the disease target and the potential of our candidate drugs in humans. Within Early Clinical Development the Study Operations organization is responsible for the delivery of planned clinical trials in accordance to agreed timelines.
Tasks and responsibilities/The role:
The Clinical Study Administrator is accountable for assisting the Associate Director Study Management (ADSM) and the Study Management Associate(s) fulfil their accountabilities through coordinating activities that ensure quality and consistency and providing administrative support. The Clinical Study Administrator will work across several clinical studies. The exact accountabilities will differ depending on the exact nature of the clinical programme so a high degree of flexibility is required.
Typical accountabilities:
• Collect, review and track relevant clinical documents, as required by the study.
• Support maintenance of the Trial Master File (TMF).
• Set-up, populate and accurately maintain information in AstraZeneca tracking and communication tools (e.g. IMPACT, ANGEL, Sharepoint, BOX) and support others in the usage of these systems
• 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 and contribute to the preparation of internal and external meetings
• Contribute to and distribute presentation material for meetings, newsletters and web-sites
Minimum requirements:
• University degree
• Basic understanding of the drug development process
• Basic knowledge of ICH-GCP principles
• Fluent in written and spoken English
• A clear demonstration of behaviours of:
o Ability to prioritise
o Flexibility
o Ability to manage multiple deliverables
o Team oriented
About the employment
For this assignment, you will be employed as a consultant by Adecco. The assignment will start immediately and initially run for 6months.
Adecco adheres to all relevant collective agreements.
Your health and wellbeing are important to us so we offer healthcare benefits, such as discount on training cards. You are also covered by insurance and occupational healthcare.
The Adecco Group is the worlds leading provider of HR solutions. With more than 32,000 FTE employees and around 5,100 branches, in over 60 countries and territories around the world, we offer a wide variety of services, connecting around 700,000 associates with our clients every day.
The services we offer fall into the broad categories of temporary staffing, permanent placement, career transition and talent development, as well as outsourcing and consulting. The Adecco Group is based in Zurich-Glattbrugg, Switzerland and we are a Fortune Global 500 company listed on the SIX Swiss Exchange.
Adecco was created in 1996, following the merger of Adia (Switzerland) and Ecco (France), two leading personnel service firms with complementary geographical profiles.
Read more at
www.adecco.comAbout the application
The assignment will be filled immediately and we are therefore recruiting on a continuous basis during the application period. Please apply through the "Ansök/Apply" button on this page and attach your CV and personal letter.
* The first step in our recruitment processes is a personality test (MAP) that will be sent to your e-mail address when your application has been reviewed. Adecco uses tests as part of the process in order insure quality and to make as fair an assessment as possible.
* If you are selected to continue to the next step in the process, you will be contacted for a telephone interview.
* The next step will be to attend a personal interview with the responsible recruiter.
Please note that in some of our processes we also use video interviews, other tests and other assessment techniques. If this is the case, you will receive information.
Contact details
If you have questions about this assignment or the recruitment process,
you are welcome to contact responsible recruiter:
Isabell Josefsson via +468 - 100 500
If you have questions regarding registration with Adecco,
please contact Adecco Candidate Support:
kandidatsupport@adecco.se alt. via tel: +468 - 598 980 10.
We look forward to receiving your application!
Keywords
Administratör, Administrator, Coordinator, koordinator, Astra Zeneca, Mölndal, Adecco, Assistant
Varaktighet, arbetstid
Heltid Visstid
Publiceringsdatum2018-10-16ErsättningFast lön
Så ansöker duSista dag att ansöka är 2018-10-21
Ange följande referens när du ansöker: ref-27892
Klicka på denna länk för att göra din ansökanKontaktIsabell Josefsson 08-100500
FöretagAdecco Sweden AB
AdressAdecco Sweden AB
Östra Hamngatan 26-28
41109 GÖTEBORG
KontorsadressÖstra Hamngatan 26-28
Jobbnummer 4404548
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