Senior Statistical Programmer
Role details
Job location
Tech stack
Job description
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, define.xml). 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: $147,022 - $202,500/year.
Requirements
Requires a master's or bachelor's degree in Computer Science, Mathematics, Statistics, Chemistry, Biochemistry or related life sciences field or foreign equivalent. Requires with master's two (2) years, with bachelor's 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 master's 2 years, if bachelor's 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.
Benefits & conditions
The potential base pay range for this role is $147,022 - $202,500 The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
