Statistical Programming Associate Director, Late Stage Respiratory
4 tygodni temu
Statistical Programming Associate Director, Late Stage Respiratory & Immunology
Location : Warsaw (PL)
Salary: Competitive, with excellent benefits.
Hybrid model of work : 3 days in office, 2 days remote per week
Reporting to: Director, Statistical Programming (Late Stage Respiratory & Immunology)
Would you like to lead clinical studies, that has direct strategic impact on drug development, playing a key role in getting medicines to patients?
At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible. We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.
Our biometrics teams use their expertise in statistics and programming to assess drug development objectives and reduce uncertainty in product development, driving better business decisions with quantitative reasoning.
What you’ll do
The Statistical Programming Associate Director provides programming expertise and mentoring to cross-function teams. This includes providing statistical programming expertise to support the design and interpretation of clinical studies and development programmes, effective management of initiatives to improve quality and integrity of information interpretation, as well as promotion of best practice and standards to enhance the value and contribution of programming across Respiratory & Immunology (R&I).
In addition to the above, the Statistical Programming Associate Director will be expected to influence and contribute to the development, sharing and support of new procedures, standards, tools, or techniques to improve quality, efficiency, and effectiveness across all areas of work.
Essential for the role
BSc or post graduate qualification (or local equivalent) in Mathematics, Statistics, Informatics, Computer Science, Life or Social Sciences Genuine commitment to drive innovation and improve efficiency Excellent interpersonal skills Extensive SAS programming knowledge Excellent knowledge of CDASH/SDTM/ADaM CDISC standards, Extensive exposure both to safety and efficacy endpoints, Experience of pharma and the life sciences and comprehensive knowledge of technical and regulatory requirements related to the role Demonstrated communication skillsDesirable for the role
Already leading studies in cross-functional environment Late stage development experience in Respiratory or Immunology Comprehensive understanding of the R&D drug development lifecycle Global Regulatory Submission experience Knowledge of /exposure to other programming languagesAt 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 ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.
Date Posted
04-cze-2024Closing Date
28-cze-2024-
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