Statistical Programmer

clinical programming team and their collection of legacy data. Leads and oversees the in-house specification and delivery of ISS and ISE datasets and associated output (tables, figures and listings) when not provided by CRO. Leads and oversees the design and implementation of complex SAS programs for applications designed to analyze and report complex clinical trial data in CDISC ADaM format. Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group. Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables. Additional tasks: * Collaborates with CR&D staff regarding data analysis requests. * Performs additional statistical analyses including but not limited to: o support responses to regulatory agencies, o generate integrated summary of safety and efficacy, o support publications and presentations, o support 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 related area with relevant experience Experience * At least 5+ years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software. * Indepth understanding of clinical programming and/or statistical programming processes and standards. * Extensive experience with statistical programming using the SAS software including development and use of SAS Macros. Strong programming and problem-solving skills. * Good experience in R Programming (Trained/Hands on experience) *Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM). * Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent). * Proven, ability to work

effectively both independently or in a team setting, and to meet set goals by managing own timelines. * Experience in working in cross-functional, multicultural and international clinical trial teams. **Why IQVIA** This role will be dedicated to one of IQVIA's largest clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique opportunity to work on a team where your role is both challenging and rewarding, while working alongside colleagues who are passionate about influencing the future of medicine and advancing therapies. With IQVIA's FSP business unit, you become a core part of a dynamic team dedicated to reshaping the future of healthcare. **Additional Benefits:** + Home-based remote work opportunities + Great work/life balance + Collaborate 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 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 IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO