Senior Statistical Programmer - Oncology (m/w/d)IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory submissions. Programming and performing related tasks serving the full spectrum of statistical programming needs in our DS3 environment (home based).ResponsibilitiesImport data from various sourcesProgram quality control checks for source data and reporting data issuesInterpret project level requirements and develop programming specificationsWrite programming code following established Good Programming PracticesProgram SDTM and ADaM datasetsProgram to create statistical analysis tables, listing and figuresValidate datasets and all statistical outputs per prescribed gate checksCommunicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and timelinesUse and promote the use of established standards, SOPs, and standard methodologiesExport data and clinical study report materialsProvide training and mentoring to team members and department staffWe offer access to cutting-edge in-house technology and opportunities to work on global projects across therapeutic areas. You will be challenged in a fast-paced, collaborative biostatistical analyses and advanced statistical programming environment. Development opportunities and mentoring are available to help you progress in your long-term career.The PersonCandidates should possess a Master’s or Bachelor’s degree in Biostatistics, Statistics, Mathematics, or Computer Science, and have strong educational or practical experience in programming.Key required skillsHome Based/Remote5+ years of experience in a Statistical Programmer role from CRO/Pharma with ADaM/SDTM/TLFsExcellent accuracy, attention to detail, problem solving, organizational and interpersonal communicationExperience in SAS programming within CRO/Pharma/Biotech/Healthcare industriesKnowledge of statistics and routine to occasionally complex analytical skillsFocus on quality, accuracy, and completeness of work activitiesExcellent communication skillsUnderstanding of Good Clinical Practice and ICH guidelinesAbility to independently lead (or have lead potential) and estimate programming scope of work, manage resource assignments, and meet project timelinesProactive, reliable, and able to work with integrityAbility to establish and maintain effective working relationships with co-workers, managers, and clientsThis role is not eligible for UK visa sponsorshipIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. Learn more at https://jobs.iqvia.com #J-18808-Ljbffr