Senior Statistical Programmer

Senior Statistical Programmer (Remote - Permanent Homebased) 3 days ago. Be among the first 25 applicants. Join to apply for the Senior Statistical Programmer (Remote - Permanent Homebased) role at IQVIA. Why IQVIA This role will be dedicated to one of IQVIA’s largest clients through a Functional Service Provider (FSP) type partnership. You’ll enjoy all the benefits of working for an industry‑leading global CRO while operating within a sponsor environment and utilizing sponsor systems. The clients include world‑class pharmaceutical and biotech companies, offering you a unique opportunity to work on challenging, rewarding projects alongside passionate colleagues who are shaping the future of medicine. Additional Benefits Home‑based remote work opportunities Great work/life balance Collaboration on projects and innovations with industry leaders in the Pharma and CRO sectors Cohesive team environment fostering a collaborative approach to study work Variety of therapeutic areas, indications and study phases Job stability; long‑term engagements and development opportunities Career advancement opportunities Job Description The Senior Statistical Programmer will be responsible for reviewing datasets in submission‑ready standard formats (ADaM), tables, figures, listings and submission packages. The role requires expertise in the design, development and quality‑control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested analyses. Main Responsibilities and Accountabilities Collaborate with study teams to design data structure and specifications for ad‑hoc and study deliverables, including ADaM datasets, tables, figures, listings and analysis submission content. Ensure the quality and accuracy of clinical data, achieving submission readiness as required by authorities (SDTM, ADaM, tables, figures, listings, define.xml). Lead and oversee pooled and exploratory analyses in close partnership with the Statistics Technical Assistant lead, study statisticians, and the clinical programming team. Lead and oversee the in‑house specification and delivery of ISS and ISE datasets and associated output (tables, figures, listings) when not provided by a CRO. Lead and oversee the design and implementation of complex SAS programs that analyze and report clinical trial data in CDISC ADaM format. Develop global tools to increase the efficiency and capacity of the Statistical Programming group. Work closely with clinical study teams to plan and execute activities that meet project timelines with high‑quality deliverables. Additional Tasks Collaborate with CR&D staff regarding data analysis requests. Perform additional statistical analyses, including: supporting responses to regulatory agencies, generating integrated summaries of safety and efficacy, supporting publications and presentations, and supporting planning and reporting of clinical trials via exploratory analyses of available data. Position Qualifications and Experience Requirements Education BSc in Computer Science, Mathematics, Statistics or a related area with relevant experience. Experience At least 5+ years of experience in clinical programming and/or statistical programming within the CRO/pharmaceutical environment, using SAS software. In‑depth understanding of clinical programming and/or statistical programming processes and standards. In‑depth understanding of regulatory requirements relevant to statistical programming (e.g., GCP, ICH). Extensive experience with statistical programming using SAS, including development and use of SAS macros; strong programming and problem‑solving skills. Advanced knowledge of CDISC standards (CDASH, SDTM, ADaM). Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities. Proven ability to work effectively both independently and in a team setting, managing timelines to meet goals. Experience working in cross‑functional, multicultural and international clinical trial teams. 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 https://jobs.iqvia.com #J-18808-Ljbffr