Role Barcelona onsite 3 days office/2 days homeSi le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación.Would you like to be part of a fast-paced and agileglobalteam that hasdirectstrategic impact on drug development, empowered and trusted to innovate and experiment?

Join us at AstraZeneca CVRM (Cardiovascular Renal Metabolism) Biometrics toimpacta wide range of engaging projects striving to make a difference for millions of patients.

Our Biometrics team consists of Statisticians,StatisticalProgrammers,Informationand DataScientists.Wedrive and contribute tooptimizedclinical drug development programs andaccess to information and scientific knowledge management.We are now offering an exciting opportunity for a dedicated and highly motivated individual to join us asStatisticalProgramming Associate Director.This roleis a delivery focusedtechnical leadership rolefor programmingand overseeingdeliverables with quality and timeliness, following established standards and processes.This leadership role requires profound programming experience and excellent industry knowledge to independently lead implementation of programming activities and guide other programmers.

You will provide subject matterexpertisewithin the Programming discipline and act as a specialist within cross-functional teams to deliver continuous improvement.This role will be placed at AstraZeneca's dynamic R&Dglobal; hubinBarcelona(Spain), where you will work in an international environment at the forefront of clinical development.AccountabilitiesAs a StatisticalProgramming Associate Director, youareresponsible forleadingand directing the full scope of projectdeliveryand/orleadatechnical project withinthe TA/Drug Project/Study/Function.Leadingimplementation 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 deliverable and/or technical subject matter expert for aspect(s) of the TA, Project, or functionLeadingor contributingto cross-functional administrative or process improvement initiative(s)Drivingthe development of best practices to improve quality, efficiency,and/or effectiveness within the functionDrivingstandards development and implementationManagingand escalatingrisk in complicated or novel situations within study and/or projectsProvidingprogrammingexpertiseto the teamProvidingtactical inputsand/or drivingideas and improvementsContributingto the function by supporting recruiting and/or providing training and mentorshipIdentifyingopportunities to improvemethodologyand provides practical solutions for problemsManagingactivities of our external partners (i.e.Contract ResearchOrganisations)Influencingstakeholders by providing subject matterexpertiseon programming related itemsEnsuringcompliancetostandards and automation usageEmployingall project management practices in managing drug or technical projectsProvidinginput to capacity management for all projects in scopeMaintainingexpertiseofthe latest industry and regulatory requirements to stay currentEducation, Qualifications, Skills, and ExperienceDegree in Mathematics (i.e., Applied Math, Engineering,etc), Statistics, Computer Science, Life Science,



or equivalentExcellent programming skills in SAS(or R)and SAS macrosThoroughknowledgeof the clinical development processThorough knowledge ofindustry standards(CDISC)and ability to implement themAbility to apply programmingexpertiseto 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 MindsetDesirable Skills/ExperienceBroad experienceacross multiple therapeutic areas andacross all phases of clinical trialsExperience in regulatory submissions and interactionsAt AstraZeneca, we believe in the potential of our people, and youwilldevelop 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.

As aStatisticalProgramming Associate Director,youwillplay a pivotal role inmakinga positive impact on changing patients' lives.This role is an office-based role with some degree of flexibility.

Our vibrant office sites provide a diverse and collaborative work environment, where interactions lead to ideas and innovations, giving you and others the perfect opportunity to learn, grow and develop careers.Date Posted04-ago-*Closing Date30-oct-*AstraZeneca 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 industry-leading 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.

xqbhyrx We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

📌 Statistical Programming Associate Director (Barcelona)
🏢 Astrazeneca
📍 Barcelona