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Position: Principal Statistical Programmer
Institution: IQVIA
Location: Manchester, United Kingdom
Duties: 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
Requirements: Minimum of 8+ years of experience in Statistical Programming in pharmaceutical or medical devices industry; 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; Thorough understanding of relational database components and theory; Must have excellent knowledge of CDISC standards (SDTM andADaM)
   
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Start right here at IQVIA. Enter Keyword Enter Location Search Jobs Principal Statistical Programmer Apply now Manchester, England Full time R1136611 Date Posted: 07/14/2020 Job description IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.Key Skills: -Must have expertise of 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 andADaM)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 8+ 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) guidelines Knowledge of statistics, programming and/or clinical drug development processAdvanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro LanguageShould have experience with SDTM Implementation andADaMimplementation 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 coworkers, 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.Fulfill 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.Join UsMaking a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.Forge a career with greater purpose, make an impact, and never stop learning. Apply now Save job Remove saved job Recently Viewed Jobs No Recently viewed jobs. View all opportunities. Explore location Share this job Twitter LinkedIn Facebook Learn more about IQVIA Our Company At IQVIA, we want to help customers take healthcare further than ever before. Life at IQVIA Our work is important. It's challenging. And we're committed to working together to make a difference. Join IQVIA’s Talent Network Register today and we'll let you know when positions that match your career interests become available. 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