Statistical Programming Associate Director - RI
Statistical Programming Associate Director - RI
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1 Vacancy
Job Description
WHY JOIN US
At AstraZeneca we are dedicated to being a Great Place to Work where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. With an ambitious goal of delivering 20 new medicines by 2030 there is no better place to make a difference in medicine for patients and in society.
Join us on this exciting journey to pioneer the future of healthcare. Our inclusive culture champions diversity and collaboration and we are always committed to lifelong learning growth and development. As part of our team youll contribute to groundbreaking advancements that will shape a healthier future for people everywhere. Be a catalyst for change at AstraZeneca where your work will have a real impact on improving peoples lives.
Recognizing the importance of individualized flexibility our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging facetoface in our offices 3 days a week. Our head office is purposely designed with collaboration in mind providing space where teams can come together to strategize brainstorm and connect on key projects.
About the Opportunity:
Our R&I Biometrics team is dedicated to the development of innovative treatment of Respiratory and Immunology (R&I) diseases. You will join a global diverse and crossfunctional environment where you will get personal and professional development.
In this role we will give you the chance to utilize your statistical programming expertise in analysis and reporting of clinical trials and exploratory analyses to manage and generate evidence to support our product portfolio.
What Youll Do:
Lead Statistical programming deliverables for regulatory submissions including specification and delivery of datasets outputs and response to regulatory questions; commercialization and reimbursements
Lead delivery of the Clinical Study Report (CSR) Study Data Tabulation Model (SDTM)/Analysis Data Model (ADaM) databases and Tables Figures and Listings (TFL) outputs through both internal and external delivery models following applicable data standards and regulations
Lead Statistical programming contribution to Development Safety Update Reports (DSUR) Periodic BenefitRisk Evaluation Report (PBRER) Investigators brochures (IB)
Contribute to or lead the statistical programming thinking analysis and reporting to relevant groups in product and study teams
Lead development of standard methodology to improve quality efficiency and effectiveness
Drives standards development implementation and measure compliance to them
Provides inputs to capacity management while supporting recruitment and skill development by providing training and mentorship
Employ good project management practices (estimation risk management status tracking) when planning and leading delivery
Hold CRO/Partners accountable for the highquality standards of their deliverables.
Essential Requirements:
You are focused on solving challenging problems through collaboration and partnerships. You are a specialist in your field or aspire to be a specialist and you know that the best results are achieved by utilizing the strengths of every individual.
Degree in Mathematics (i.e. Applied Math Engineering etc. Computer Science Statistics Life Sciences or similar area
Extensive experience in clinical drug development or healthcare
Advanced SAS Programming CDISC standards knowledge and industry best practices
Excellent interpersonal skills
SO WHATS NEXT
To be considered for this exciting opportunity please complete the full application on our website at your earliest convenience it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit please share this posting with them.
Great People want to Work with us! Find out why:
Are you interested in working at AZ apply today!
AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment assessment and selection process and may be requested by emailing.
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Date Posted
24Mar2025Closing Date
27Apr2025AstraZeneca 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 industryleading 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 nondiscrimination in employment (and recruitment) as well as work authorization and employment eligibility verification requirements.
Required Experience:
Director
Employment Type
Full-Time
