The Statistical Programming Associate Director is accountable for quality, timely and efficient delivery of project programming work and good information management. This position requires profound programming experience and excellent industry knowledge to independently lead implementation of programming activities as well as lead other programmers. It is a leadership role that can have a project or technical focus. It will provide subject matter expertise within the Programming discipline. As an expert within their own field, acts as a specialist within cross-functional teams to deliver continuous improvement.
Accountabilities Leads and directs the full scope of project delivery and/or leads a technical project within the TA/Drug Project/study/function Leads Implementation of statistical programming aspects of the protocol or clinical development program Responsible for the high quality of all project deliverables, holding partners and providers accountable for the quality of their deliverable and/or technical subject matter expert for aspect(s) of the TA, Project, or function Leads or contribute to cross-functional administrative or process improvement initiative(s) Drives the development of best practices to improve quality, efficiency and/or effectiveness within the function Drives standards development and implementation Manages and escalates risk in complicated or novel situations within their study and/or projects Provides Programming expertise to the team Provides tactical input and/or drives ideas and improvements Contributes to the function by supporting recruiting and/or providing training and mentorship Identifies opportunities to improve methodology and provides practical solutions for problems Manages activities of our external partners (i.e. Contract Research Organisations) Influences stakeholders by providing subject matter expertise on programming related items Ensures compliance to standards and automation usage Employs all project management practices in managing drug or technical projects Provides input to capacity management for all projects in scope Maintains expertise of the latest industry and regulatory requirements to stay current. Essential Skills/Experience: Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science or equivalent Proven programming expertise Thorough knowledge of the clinical development process Thorough knowledge of industry standards and ability to implement them Ability to apply programming expertise to problem solving and troubleshooting for teams Current knowledge of technical and regulatory requirements relevant for the role Ability to proactively manage concurrent activities within a project Proficient ability to influence relevant stakeholders on programming related items Ability to manage risk in complicated or novel situations Project Mindset Desirable Skills/Experience: Experience in problem solving and conflict resolution skills. Why AstraZeneca? At AstraZeneca's Biopharmaceuticals R&D division, you will play an essential role in helping patients who need it the most. There is no better place to apply your Biometrics expertise in a new and different way. Here, we don't accept the status quo, digging deep to see what the data is telling us, using cutting-edge methodologies and models to drive scientific breakthroughs. Our supportive, yet challenging, approach makes for an inspiring learning environment. Every setback is seen as a chance to improve, every critique pushes us towards the next ground-breaking solution. We are always expanding our knowledge to get a broad perspective. It allows us to leverage and fuse our own skills with others to maximise impact.
Ready to make a profound impact with research that makes a clear and tangible difference? Apply today and join us in our mission to fuse science and data for the betterment of patients worldwide!
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