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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 |
Clinical Information Science - PrincipalLocation – Cambridge (UK)At AstraZeneca our Oncology Biometrics department is an integral part of the Oncology R&D organisation. We drive excellent design in order to generate the appropriate data needed for quality decision making. The goal of Oncology Biometrics is to deliver value to the pipeline by excellence in delivery, improved decision making and engaging and shaping the external environment whilst accessing and implementing innovative solutions. Would you like to be a part of helping us achieve this ambition Explore the possibility of joining us as a Clinical Information Science, Principal within Oncology.Would you like to be a part of helping us achieve this ambition Explore the possibility of joining us as a Clinical Information Science Principal (CISP) within Oncology & Immuno-Oncology.Even as research and development continues to break boundaries in how we understand and fight cancer, there are still more than eight million lives lost every year to the disease. This is why the optimal use of clinical information to shape our trials and subsequent portfolio of oncology products is crucial to us being able to deliver life-changing medicines to patients most in need. Would you be motivated to join us in our dedication to the cause of one-day helping to eliminate cancer as a cause of deathRoleIn this role you will support global clinical directors and trial design teams in finding and structuring clinical information driving optimal designs for late stage oncology drug development. It sits within our Information Practice unit who enterprise reuse of clinical information and knowledge retention for better informed decision-making and clinical development.ResponsibilitiesEmbedded within dynamic oncology drug project teams, you will ascertain and deliver the information clinical teams need to assist them in making decisions driving the drug development process. For example, using a variety of information sources such as ClinicalTrials.Gov, BioMed Tracker, and internal clinical databases.You will also contribute to key drug meetings and committees by establishing the scope, goals and deliverables supporting business goals in collaboration with senior management and decision makers.The significant areas for contribution are:Clinical Design