Associate Director /Director

h3Associate Director, Statistical Programming (w/m/d) /h3 pCSL Behring AG Vacant since : Number of jobs : 1 8152 Glattbrugg (ZH) 100% Immediately Permanent /p pThe Associate Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with the Director, Statistical Programming to ensure all assigned Statistical Programming tasks are managed to completion. Work closely with Statisticians to ensure that deliverables provided by internal resources or outside providers (CROs; FSP providers) are accurate and aligned with CSL standards. /p pThis individual may manage a Therapeutic Areas (TA) or programs within or across TAs working with the Statistics TA lead to ensure all work required in the TA is completed within the project timelines with high quality. /p h3Main Responsibilities and Accountabilities /h3 ul lipWorking with the Director, Programming to assess upcoming activities and resulting resource needs and ensure high quality, timely, delivery of assigned projects. Ensure realistic project planning. /p /li lipOversee the CRO delivery or manage the in-house programming of data sets, outputs, and DDT files of clinical trials and integrated analysis. /p /li lipPlans and leads the design and implementation of complex specifications and programs for applications designed to analyze and report complex clinical trial data in CDISC format. /p /li lipCoordinating the oversight or in-house programming of exploratory analyses, analyses to support secondary publications, response to regulatory requests, or other adhoc requests. /p /li lipMentors programmers allocated to assigned projects and provides feedback to managers of these team members as needed. /p /li lipAs a project or program leader ensures compliance with programming process and strategy to facilitate accurate and timely programming. /p /li lipTest and implement state of the art programming methods and tools to the organization and drive automation of delivery, including AI. /p /li /ul h3Education /h3 ul lipBSc in Computer Science, Mathematics, Statistics or related area with relevant experience /p /li lipOther degrees and certifications considered if commensurate with related programming experience /p /li /ul h3Experience /h3 ul lipAt least 9 years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software. /p /li lipComprehensive understanding of clinical programming and/or statistical programming processes and standards. /p /li lipAdvanced Experiences with statistical programming using the SAS software including development and use of SAS Macros. /p /li lipAdvanced knowledge in CDISC standards (CDASH, SDTM, ADaM). /p /li lipProven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines. /p /li lipExperience in working in cross-functional, multicultural and international clinical trial teams. /p /li /ul h3Competencies /h3 ul lipCoding in SAS, including SAS macro language /p /li lipInterest and/or experience in expanding beyond SAS as the primary programming delivery tool /p /li lipExperience in and/or passion for automatization of routine programming tasks /p /li lipBroad knowledge of clinical development and processes /p /li lipStrong interpersonal and communication skills (verbal and written in English), comfortable around senior management /p /li lipAbility to collaboratively work in matrix environment /p /li lipA solutions oriented mindset /p /li lipFluency in technical requirements for CDISC compatible datasets and DDT files /p /li lipPresentations of programming techniques at professional conferences is a plus /p /li /ul h3Work Information /h3 ul liWork location 8152 Glattbrugg (ZH) /li liWorkload 100% /li liEmployment start Immediately /li liEmployment duration Permanent /li /ul h3Language Skills /h3 ul liEnglish Orally : Very good knowledge Written : Very good knowledge /li /ul h3Contact /h3 ul liBy email /li /ul #J-18808-Ljbffr