Principal Statistical Programmer

Location: Homebased anywhere in the USPurpose:Join our FSP team today! In this role you will plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.Job Details:Position: – Principal Statistical ProgrammerHome BasedMin 4+ years of CRO/Pharma IndustryTherapeutic Areas: Oncology // Immunology // IDV // EDCPKey Skills:Must have expertise of R programming as well as SAS® Base, and good knowledge of SAS® graph and SAS® Macros.Capable of implementing more advanced statistical procedures as per specifications provided by biostatistician.Must have excellent knowledge of CDISC standards (SDTM and ADaM)Thorough understanding of relational database components and theory.Excellent application development skills.Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.Good understanding of ICH E6, ICH E3, ICH E8, ICH E9 and clinical research processes.Minimum of 4+ years of experience in Statistical Programming in pharmaceutical or medical devices industryGood verbal and written communication skills.Ability to work on multiple projects, plan, organize and prioritize activities.Required Knowledge, Skills and Abilities:Experience as technical team lead directly engaging clients and coordinating tasks within a programming teamIn-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelinesKnowledge of statistics, programming and/or clinical drug development processAdvanced knowledge of R programmingBase SAS, SAS/STAT, SAS Graph and SAS Macro LanguageShould have experience with SDTM Implementation and ADaM implementation according to CDISC Standards.Must have expertise in SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL.Good organizational, interpersonal, leadership and communication skillsAbility to independently manage multiple tasks and projectsAbility to delegate work to other members of the SP teamExcellent accuracy and attention to detailAbility to delegate work to other members of the SP team [SPM]Exhibits routine and occasionally complex problem-solving skillsAbility to lead teams and projects and capable of managing at a group levelRecognizes when negotiating skills are needed and seeks assistance.Ability to establish and maintain effective working relationships with co-workers, managers and clients.Responsibilities:Perform, plan co-ordinate and implement the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing and (ii) the programming of analysis datasets (derived datasets) and transfer files

for internal and external clients and (iii) the programming

quality control checks for the source data and report the data issues periodically..Ability to interpret project level requirements and develop programming specifications, as appropriate, for complex studies.Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies.Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.Use and promote the use of established standards, SOP and best practices.Provide training and mentoring to SP team members and Statistical Programming department staff.MINIMUM REQUIRED EDUCATION AND EXPERIENCE:Bachelor's degree from reputable university preferably in science/ mathematics related fieldsIQVIA 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.comWe are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoeIQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-statusThe potential base pay range for this role, when annualized, is $117,400.00 - $218,000.00. 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.