Senior Statistical Programmer Global BiostatisticsHome-based, office-based, hybrid options available Join us on ourexciting journey! The Global Biostatistics (Data Sciences, Safety& Medical) team at IQVIA are experienced in submissions for allmajor regions; working together with key groups such as GlobalRegulatory Affairs, Safety, Project and Data Management, andMedical Writing, to drive efficiency and accountability. IQVIABiostatistics helps interpret and draw inferences from datacollected on patients as they progress through a clinical trial andserves as the bridge between data capture and reporting. We haveone of the largest Biostatistics departments within the industry ofaround 1,100+ staff, to which we engage the full range ofindustry-leading resources and expertise spanning all study phasesand therapeutic areas. Job Overview: As a Senior StatisticalProgrammer, you will be given access to cutting-edge, in-housetechnology and opportunities to work on global projects across avariety of therapeutic areas. Thanks to our developmentopportunities and mentoring at all levels, you will be able toprogress your long-term career in the direction you choose. Youwill provide experienced technical expertise to develop processmethodology for the department to meet internal and externalclients’ needs. You will plan and coordinate the development ofintegrated programming solutions, serving the full spectrum ofstatistical programming needs, along with providing technicalexpertise and leadership to the department and providing internalconsulting services, including specifications and user needsanalysis for complex project or client requirements. Acting as alead on studies, you will directly communicate with internal andclient statisticians and clinical team members to ensureappropriate understanding of requirements and project timelines andsupport the training of new or junior team members. You willestimate programming scope of work, manage resource assignments,communicate project status, and negotiate/re-negotiate projecttimelines for deliverables. Requirements: - Bachelors or Masters’in Computer Science, Mathematics or equivalent - 5+ yearsStatistical Programming experience within the Life-Science industry- Experience in SAS Base, and good knowledge of SAS graph and SASMacros - Excellent knowledge of CDISC standards (SDTM and ADaM) -Excellent application development skills - Strong understanding ofclinical trial data and extremely hands-on in data manipulations,analysis and reporting of analysis results. - Experience astechnical team lead, directly engaging clients and coordinatingtasks within a programming team - In-depth knowledge of applicableclinical research regulatory requirements, i.e. Good ClinicalPractice (GCP) and International Conference on Harmonization (ICH)guidelines Join IQVIA to see where your skills can take you -Global exposure - Variety of therapeutic areas - Collaborative andsupportive team environment - Access to cutting-edge andinnovative, in-house technology - Excellent career development andprogression opportunities - Work-Life Balance, with a strong focuson a positive well-being Unleash your potential! It takes passionto make the extraordinary possible for patients. Our culture ofinnovation and collaboration enables us to explore newpossibilities and help improve health around the world. When youjoin our diverse, global team, you’ll harness the power ofunparalleled data, advanced analytics, cutting-edge technologies,and deep healthcare and scientific expertise to drive healthcareforward. #J-18808-Ljbffr
