Skills this job asks for
StatisticsLeadershipProject managementRisk management
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About the role
Are you an experienced Statistical Programming professional with deep knowledge of clinical drug development? Would you like to use your technical expertise to provide strategic programming leadership and help shape the delivery of clinical development programmes? Join us at AstraZeneca CVRM (Cardiovascular Renal Metabolism) Biometrics to impact a wide range of engaging projects striving to make a difference for millions of patients. Our Biometrics team consists of Statisticians, Programmers, Information and Data Scientists. We drive and contribute to optimized clinical drug development programs and access to information and scientific knowledge management.
We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us as Statistical Programming, Associate Director, providing strategic programming leadership within CVRM Biometrics and collaborating with global product development teams.
This role is primarily focused on strategic and technical leadership, planning and project management rather than hands-on statistical programming. You will draw on your technical programming expertise to provide direction, oversee delivery and support high-quality decision-making.
This role will be placed at AstraZeneca’s dynamic R&D strategic site in Gothenburg (Sweden), where you will work in an international environment at the forefront of clinical development.
Accountabilities:
As a Statistical Programming, Associate Director , you are accountable for quality, timely and efficient delivery of project programming work and information management. This position requires profound programming experience and excellent industry knowledge to provide strategic and technical leadership across programming activities, including planning and project management. This is a strategic leadership role with project and technical focus where you will provide subject matter expertise within the statistical programming discipline. You will oversee the delivery of data according to industry standards, and high-quality statistical analyses and reporting deliverables, as well as planning and execution of submission strategies. You will act as a specialist within cross-functional teams to drive continuous improvement, innovation, and automation solutions.
Essential Skills/Experience:
• Degree in Mathematics (e.g., Applied Math, Engineering, etc.), Statistics, Computer Science, Life Science, or equivalent experience
• Advanced knowledge of the clinical development process and industry standards
• Demonstrated programming leadership capability, with the ability to provide strategic and technical direction, develop teams and individuals, and lead them towards a common goal without formal line management responsibility
• Demonstrated influencing, planning and organizational skills
• Ability to provide input to functional strategies
• Expertise in risk management in complex or novel situations
• Strong technical experience in SAS and CDISC standards, together with current knowledge and awareness of regulatory requirements relevant to Statistical Programming
Desirable Skills/Experience:
• Broad experience, ideally across multiple therapeutic areas and/or beyond Statistical Programming
• Experience in regulatory submissions and regulatory interactions
• Demonstrated experience in designing and implementing business processes
• Willingness and ability to travel
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. In this role, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changin
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