Senior Statistical Programmer

Senior Statistical Programmer (Multiple Openings) IQVIA RDS Inc. Durham NC. May telecommute (work from home) from anywhere in U.S. and report to Durham NC work location. Collaborate with the study statistician to design data structure and specifications for ad hoc and study deliverables including but not limited to ADaM datasets tables figures Listings and Analysis Submission content. Lead the production and validation efforts for the designed output which may include oversight of work by CROs. Collaborate with peers and statisticians to ensure the quality and accuracy thus submission readiness of clinical data as required by authorities (i.e. SDTM ADaM tables figures listings ). Support the review of related deliverables when provided by CROs. Lead requested efforts for pooled and exploratory analyses working closely with clinical programming team and their collection of legacy data. Lead the in-house specification and delivery of ISS and ISE datasets and associated output (tables figures and listings) when not provided by CRO. Lead the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format. Identify problems and develop global tools that increase the efficiency and capacity of the Statistical Programming group. Work closely with clinical study teams to ensure that project timelines are met with high quality deliverables. Support CR&D staff in data analysis requests. Perform additional statistical analyses including but not limited to: support responses to regulatory agencies generate integrated summary of safety and efficacy support publications and presentations support planning and reporting of clinical trials via exploratory analyses of available data and replicate statistician analyses for QC. Work M-F 8:30am 5:30pm EST. Salary Range: $147022 $202500/year.

Requires a masters or bachelors degree in Computer Science Mathematics Statistics Chemistry Biochemistry or related life sciences field or foreign equivalent. Requires with masters two (2) years with bachelors four (4) years of experience in clinical programming or statistical programming utilizing SAS software including development and use of SAS Macros within the CRO or pharmaceutical environment to include (if masters 2 years if bachelors 4 years) the following: utilizing knowledge of clinical programming or statistical programming processes and standards; utilizing knowledge of CDISC standards (CDASH SDTM or ADaM); and working in cross-functional multicultural and international clinical trial teams. Apply: reference job #118692.

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

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