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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 |
At AstraZeneca want to redefine the cancer-treatment paradigm, our broad pipeline of next-generation medicines is focused principally on four disease areas – breast, ovarian, lung and haematological cancers, and we aim to bring six new cancer medicines to patients by 2020.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 play a leading role in supporting 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.In Biometrics & Information Sciences (B&I) we are the statistical and information experts for late stage (phase II and beyond) drug development. You’ll be part of a truly global team alongside some of the most respected statistical programming, information practice and analytics specialists in the industry.ResponsibilitiesAs a strategic director embedded within dynamic oncology drug project teams, you will lead the delivery of 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 lead key drug meetings and committees by establishing the scope, goals and deliverables supporting business goals in collaboration with senior management and decision makers. This will include developing and controlling deadlines as well as preparing progress reports.The significant areas for contribution are:Clinical Design