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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 |
Job Title: Associate Director of Clinical Development, OncologyLocation: Cambridge, UKSalary: AstraZeneca offers a competitive salary and benefits packageAt AstraZeneca when we see an opportunity for change, we seize it and commit real resources to make it happen, because an opportunity no matter how small can be the start of something big. Delivering life-changing medicine is about being entrepreneurial - finding those moments and recognizing their potential. Big success can come from seeing potential in something. We empower our people to seek these out, and we support them to pursue the opportunities they find !Late Stage Oncology is the science engine room for our late stage development. Our strategy and ability to transform our portfolio means we have a late stage pipeline that presents opportunities to push the boundaries of science to deliver medicines. We transform clinical concepts into medicines that deliver patient health benefits !The Associate Director of Clinical Development (ADCD) is a core global role within the Clinical Operations function of Late Stage R&D (BioPharmaceuticals and Oncology). The span of responsibilities is broad and may support one or several products depending on their size and complexity. The products supported will be in Phase 3 development or on the Market, but the program may include studies in all phases of drug development.You will be responsible for oversight of a program of global studies, covering all clinical development deliverables (including aspects of quality, budget, time, resource and risk). The role also involves integrating design, feasibility and operational planning to ensure clinical drug development programs are aligned with priorities and strategy.You will provide input & support to the Director of Clinical Development (DCD) in preparation for governance interactions. Acting Lead for cross-functional teams in delivery of clinical activities assigned (e.g. indication specific sub-teams, Investigator Brochure production, DSUR etc)Additionally, youll provide project leadership & management for cross-functional clinical submission teams in support of regulatory marketing applications and post registration product maintenance phases. Requirements