PpThe Associate Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of CSL’s statistical programming capabilities required to meet regulatory obligations. The individual works closely with the Director, Statistical Programming to ensure all assigned Statistical Programming tasks are managed to completion and that deliverables provided by internal resources or outside providers (CROs; FSP providers) are accurate and aligned with CSL standards. /p h3Main Responsibilities And Accountabilities /h3 ul liWork with the Director, Programming to assess upcoming activities and resulting resource needs and to ensure high quality, timely delivery of assigned projects, including realistic project planning. /li liOversee or manage the CRO delivery or in‑house programming of data sets, outputs, and DDT files of clinical trials and integrated analyses. /li liPlan and lead the design and implementation of complex specifications and programs for applications designed to analyze and report complex clinical trial data in CDISC format. /li liCoordinate the oversight or in‑house programming of exploratory analyses, analyses to support secondary publications, responses to regulatory requests, or other ad‑hoc requests. /li liMentor programmers allocated to projects and provide feedback to managers of these team members as needed. /li liAs project or program leader, ensure compliance with programming processes and strategy to facilitate accurate and timely programming. /li liTest and implement state‑of‑the‑art programming methods and tools, including automation of delivery and use of AI. /li /ul h3Education /h3 ul liBSc in Computer Science, Mathematics, Statistics or related area with relevant experience. /li liOther degrees and certifications considered if commensurate with related programming experience. /li /ul h3Experience /h3 ul liAt least 9 years of experience in clinical and/or statistical programming within the CRO/pharmaceutical environment using SAS software. /li liComprehensive understanding of clinical programming and or statistical programming processes and standards. /li liAdvanced experience with statistical programming using SAS, including development and use of SAS macros. /li liAdvanced knowledge of CDISC standards (CDASH, SDTM, ADaM). /li liProven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines. /li liExperience working in cross‑functional, multicultural and international clinical trial teams. /li /ul h3Competencies /h3 ul liCoding in SAS, including SAS macro language. /li liInterest or experience in expanding beyond SAS as the primary programming delivery tool. /li liExperience or passion for automation of routine programming tasks. /li liBroad knowledge of clinical development and processes. /li liStrong interpersonal and communication skills (verbal and written in English), comfortable around senior management. /li liAbility to collaborate in a matrix environment. /li liA solutions‑oriented mindset. /li liFluency in technical requirements for CDISC compatible datasets and DDT files. /li liPresentations of programming techniques at professional conferences is a plus. /li /ul h3Our Benefits /h3 pFor more information on CSL benefits visit How CSL Supports Your Well‑being | CSL. /p h3Equal Opportunity Employer /h3 pCSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit /p /p #J-18808-Ljbffr