Statistical Programming Associate Director

Statistical Programming Associate DirectorThe 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.LOCATION: Durham, NCAccountabilities: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 programResponsible for the high quality of all project deliverables, holding partners and providers accountable for the quality of their deliverables and/or technical subject matter expert for aspect(s) of TA, Project, or functionLeads 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 functionDrives standards development and implementationManages and escalate risk in complicated or novel situations within their study and/or projectsProvides Programming expertise to the teamProvides tactical input and/or drives ideas and improvementsContributes to the function by supporting recruiting and/or providing training and mentorshipIdentifies opportunities to improve methodology and provides practical solutions for problemsManages activities of our external partners (i.e. Contract Research Organisations)Influences stakeholders by providing subject matter expertise on programming related itemsEnsures compliance to standards and automation usageEmploys all project management practices in managing drug or technical projectsProvides input to capacity management for all projects in scopeMaintains expertise of the latest industry and regulatory requirements to stay currentRequired Skills:Degree in Mathematics (i.e., Applied Math, Engineering, etc), Statistics, Computer Science, Life Science or equivalentProven programming expertise Thorough knowledge of clinical development processThorough knowledge of industry standards and ability to implement themAbility to apply programming expertise to problem solving and troubleshooting for teamsCurrent knowledge of technical and regulatory requirements relevant for the roleAbility to proactively manage concurrent activities within a projectProficient ability to influence relevant stakeholders on programming related itemsAbility to manage risk in complicated or novel situationsProject MindsetDesired Skills:Demonstrated planning and organizational skillsWhen we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.The annual base pay (or hourly rate of compensation) for this position ranges from $137,135 to $205,703. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.Why AstraZeneca:Here you will contribute to a bold mission to transform outcomes for people by advancing earlier detection and smarter, faster trials. You will operate at the intersection of innovative science and technology, backed by significant investment and an empowered, collaborative culture that brings clinicians, scientists, and data experts together to accelerate breakthroughs. We value kindness alongside ambition, giving you the trust, tools, and cross-functional partnerships to lead with confidence and shape studies that matter—so your decisions today translate into meaningful patient impact tomorrow.Call to Action:Step into this country leadership role to accelerate life-changing trials and turn bold science into results that matter—make your move and help shape what comes next.