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Job Location | Cambridge |
Education | Not Mentioned |
Salary | Competitive salary |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent, full-time |
Do you have experience in clinical study management and would like a role where your expertise, as well as your leadership skills, will be highly appreciated Are you team oriented and do you, as we do, put patients first in your work to make a difference Then AstraZeneca might be the right place for you to contribute and thrive. We are recruiting for a Global Study Manager who will join our BioPharmaceuticals R&D Study Management Early team - as a part within the Development Operations function. The position will be based on one of our vibrant R&D sites in Gothenburg, Sweden; Granta Park, UK or Gaithersburg, US.In the position as Global Study Manager you will support the delivery of global early clinical studies from study set-up through maintenance, close-out and study archiving. It is a role where you work cross-functionally with internal and external partners to lead and deliver aspects of the clinical study according to applicable trial regulations (ex ICH-GCP), AstraZeneca Standard Operating Procedures (SOPs), and in line with AstraZeneca’s policies and values.BioPharmaceuticals Study Management Early, are accountable for delivering high quality, cost efficient early phase clinical studies (phase 1 to phase 2b) that support drug development within Cardiovascular Renal Metabolism (CVRM), Respiratory & Immunology (R&I) and Infectious Disease.What you’ll do:In the position as Global Study Manager you will play a key role in the study team and work close with the Global Study Leader to fulfil their accountabilities through coordinating activities that ensures quality, consistency and integration of study data. You will maintain and facilitate interactions with both internal & external functions to provide oversight and ensure efficient study delivery to time, costs and quality objectives, in both internally-run and outsourced studies. The exact accountabilities will differ depending on the exact nature of the clinical program so a high degree of flexibility is required.The responsibilities will also include: