Statistical Programming Associate Director, Late Stage Respiratory
2 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)
Excited about leading clinical studies with a direct strategic impact on drug development, playing a crucial role in delivering medicines to patients?
At AstraZeneca, we have strong faith in the potential of our team members, enabling you to grow beyond your expectations. We harness your skills and enthusiasm by actively encouraging you to explore your full potential no matter your starting point with us.
Our biometrics teams leverage their statistical and programming expertise to evaluate drug development goals, mitigating uncertainties in product development and steering better business decisions through quantitative analysis.
What you'll do
The Statistical Programming Associate Director offers programming proficiency and guidance to cross-functional teams. This involves supplying statistical programming knowledge to facilitate the design and analysis of clinical studies and development programs, efficient management of initiatives to enhance information interpretation quality and integrity, as well as advocacy of best practices and standards to elevate the value and contribution of programming within Respiratory & Immunology (R&I).
In addition to the aforementioned responsibilities, the Statistical Programming Associate Director will be tasked with influencing and participating in establishing, sharing, and endorsing new procedures, standards, tools, or techniques to enhance quality, productivity, and efficiency across all work domains.
Essential for the role
- BSc or postgraduate degree (or local equivalent) in Mathematics, Statistics, Informatics, Computer Science, Life, or Social Sciences
- Demonstrated dedication to drive innovation and enhance efficiency
- Outstanding interpersonal abilities
- Extensive SAS programming expertise
- Thorough understanding of CDASH/SDTM/ADaM CDISC standards
- Significant exposure to both safety and efficacy endpoints
- Background in pharmaceuticals and life sciences with extensive familiarity of technical and regulatory requisites linked to the position
- Proven communication skills
Desirable for the role
- Prior experience in leading studies in a cross-functional setting
- Experience in late-stage development within Respiratory or Immunology
- Comprehensive comprehension of the R&D drug development lifecycle
- Global Regulatory Submission experience
- Knowledge of/exposure to other programming languages
When AstraZeneca identifies an opportunity for change, we embrace and actualize it because every opportunity, regardless of size, could be the genesis of something significant. Delivering transformative medications necessitates an entrepreneurial spirit – identifying those instants and realizing their potential. Accompany us on our journey to establish a novel organizational paradigm that resets the standards of what a biopharmaceutical corporation can represent. This indicates that we are revolutionizing our work approaches, leading innovative strategies, and uniting unexpected teams. Interested in being a part of this journey?
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