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Principal Statistician/Associate Director Early phase Respiratory & Immunology R&I

Job LocationCambridge
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Principal Statistician/Associate Director – Early phase Respiratory & Immunology (R&I)Location: Cambridge, UKCompetitive salary plus benefits Description Would you like to be a part of a Biostatistical group, who has direct strategic impact on drug development, playing a key role in getting medicines to patientsAt AstraZeneca we’re driving leading-edge approaches to drug development across many business areas – within Early Biometrics & Statistical Innovation (EB&SI) a data-centric focus is helping us work more efficiently and creatively to bring the right medicines to the right patients. Our biometrics teams use their expertise in statistics and programming to answer drug development objectives and reduce uncertainty in product development, driving better business decisions with quantitative reasoning.We are currently looking for an experienced Principal/Associate DirectorStatistician to work at the heart of our early-phase clinical project teams. Your proven statistical expertise will be a key influence on our clinical programme designs, informing our decision making and driving best practice.The Principal Statistician/Associate Director of Statistics sits within our Early Biometrics groups in EB&SI, aligned to Respiratory & Immunology (R&I), and is responsible for providing statistical expertise to support the development programs for our compounds, including collaboration with Late Biometrics groups in R&I, along with contributions to the design and interpretation of early clinical studies and related regulatory interactions .Working as part of Data Science and AI, you’ll be able to access technology at the forefront of science in a creative environment, where you will have the scope to shape the way we work and develop new statistical ideas and approaches applied in early clinical trial research. . Main duties and responsibilities Joining a team of statistical and programming experts working in early clinical development, you will be expected to provide strategic direction as you work to bring robust quantitative thinking to the drug development cycle. Youll play a pivotal role in channelling our scientific capabilities to make a positive impact on changing patients lives.The Principal Statistician/Associate Director of Statistics will provide leadership on the project and portfolio level, bringing statistical expertise to the design, analysis, and interpretation of early phase clinical studies, and positioning the early development program to provide clear and actionable evidence for program level decision-making including late development study design. You also will provide support to regulatory submissions including specification of overview documents and response to regulatory questions. Additionally you will provide leadership to diverse initiatives to drive scientific innovation and best practice. In addition to the above, you will

  • Contribute to the development, sharing and statistical support of new procedures, standards, tools, or techniques to surpass quality, efficiency, and effectiveness within EB&SI.
  • Build opportunities for the application of modelling and simulation to improve study design, methodology and solutions for clinical development, and statistical methodology to improve and provide practical solutions for research/ production activities
  • Coach more junior staff and support with education and training of statistics staff
  • Interact with and influence key stakeholders and governance
  • RequirementsEssential
  • MSc or PhD degree in Statistics, Biostatistics, or related quantitative fields, or equivalent course work/ technical experience with experience in pharma/healthcare or other relevant area
  • In depth knowledge of the technical and regulatory requirements related to the role
  • Extensive experience of pharmaceutical development, program design and data analysis and interpretation
  • Experience of major regulatory interactions and/or submissions
  • Excellent communication skills and ability to build strong relationships
  • Excellent collaboration required – needs the energy to work across global & functional boundaries both internally and externally
  • Ability to apply statistical expertise to complex problems, problem solving and quality focus
  • Next Steps – Apply today We would like to know more about you. If you are interested, apply now!At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested Come and join our journey.AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.

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