London Jobs |
Manchester Jobs |
Liverpool Jobs |
Nottingham Jobs |
Birmingham Jobs |
Cambridge Jobs |
Glasgow Jobs |
Bristol Jobs |
Wales Jobs |
London Jobs |
Manchester Jobs |
Liverpool Jobs |
Nottingham Jobs |
Birmingham Jobs |
Cambridge Jobs |
Glasgow Jobs |
Bristol Jobs |
Wales Jobs |
Oil & Gas Jobs |
Banking Jobs |
Construction Jobs |
Top Management Jobs |
IT - Software Jobs |
Medical Healthcare Jobs |
Purchase / Logistics Jobs |
Sales |
Ajax Jobs |
Designing Jobs |
ASP .NET Jobs |
Java Jobs |
MySQL Jobs |
Sap hr Jobs |
Software Testing Jobs |
Html Jobs |
Job Location | Cambridge |
Education | Not Mentioned |
Salary | Competitive salary |
Industry | Not Mentioned |
Functional Area | Not Mentioned |
Job Type | Permanent, full-time |
Clinical Information Team LeadLocation – 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 Team Lead within Oncology.Main Duties and responsibilities As Clinical Information Science Team Lead (CITL) within the Oncology Information Practice (IP) embedded within dynamic oncology drug project teams you will lead and direct the clinical information work required in making decisions driving the drug development process and line manage a team. You will work collaboratively with both OBM drug project team leaders and drug project members along with cross functional teams. You will also lead IP department as an integral part of the Oncology IP department by establishing IP’s scope of services, goals and deliverables and support business goals in collaboration with senior management and decision makers to oversee and deliver information supporting clinical development and improve our ways of working. You will provide support for regulatory submissions including development of the information submission.Ultimately, the Oncology IP department delivers information, data and tools to support internal decision making, regulatory submissions for the portfolio of drug projects within the Oncology R&D organisation.The significant areas for contribution are:Clinical Design