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Statistical Programming Associate Director, Late Stage Respiratory & Immunology
  • Warsaw
Statistical Programming Associate Director, Late Stage Respiratory & Immunology
Warszawa, Warsaw, Masovian Voivodeship, Polska
TN Poland
25. 2. 2025
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Statistical Programming Associate Director, Late Stage Respiratory & Immunology, Warsaw

Client:

Location:

Warsaw, Poland

Job Category:

Other

EU work permit required:

Yes

Job Reference:

f16c7831d25c

Job Views:

26

Posted:

23.01.2025

Expiry Date:

09.03.2025

Job Description:

Statistical Programming Associate Director, Late Stage Respiratory & Immunology

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 have a 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-functional 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 practices 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 in pharma and the life sciences and comprehensive knowledge of technical and regulatory requirements related to the role
  • Demonstrated communication skills

Desirable for the role

  • Already leading studies in a 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 languages

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 recognizing their potential. Join us on our journey of building a new kind of organization 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.

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