www.acad.jobs : academic jobs worldwide – and the best jobs in industry
                
     
Position: Senior Statistical Programmer
Institution: IQVIA
Location: Reading, Berkshire, 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
Requirements: Minimum of 5+ years of experience in Statistical Programming in pharmaceutical or medical devices industry; 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 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
   
Text: Skip to main content Home Careers Search Results Job Description Select a Topic See all jobs Our Company Life at IQVIA Clinical Research Associates AI & Machine Learning Talent Network Saved Jobs 0 Menu Solutions Research & Development Overview Clinical Trials Functional Services Virtual Trials Consulting Real World Evidence Overview Real World Data and Insights Study Design Platforms Evidence Networks Health Economics & Value Regulatory and Safety Commercialization Overview Launch Strategy and Management Brand Strategy and Management Pricing and Market Access Healthcare Professional Engagement Patient Engagement Promotional Strategy Integrated Global Compliance Overview Safety Pharmacovigilance Regulatory Compliance Quality Compliance Commercial Compliance Technologies Overview Clinical Acceleration Patient Engagement Content Management Customer Engagement Safety Regulatory & Quality Performance Management & Insights Information Management Partner Programs Industry Segments Overview Pharmaceutical Manufacturers Emerging Biopharma Consumer Health MedTech Generics Information Partner Services Public Health and Government Patient Associations Payers Providers Featured Capabilities Human Data Science Cloud Innovative Models Overview Artificial Intelligence and Machine Learning Virtual Research Genomics Digital Health Therapeutic Areas Overview Oncology Rare Diseases Central Nervous System Infectious Diseases and Vaccines GI and Hepatology Diabetes Pediatrics Biosimilars COVID-19 Resources Insights IQVIA Insights Points of View IQVIA Institute About Our Story Human Data Science IQVIA CORE Executive Team Contact Investors News Events Privacy Careers Global Site Americas Argentina Brazil Brazil (English) Brasil (Português) Canada Canada (English) Canada (Français) Colombia Mexico Mexico (English) México (Español) United States Europe, Middle East & Africa Belgium Belgium (English) Belgique (Français) België (Nederlands) Czech Republic Czech Republic (English) Czech Republic () Denmark España Finland France France (English) France (Français) Deutschland Greece Greece (English) Ελλάδα (Ελληνικά) Ireland Israel Italy Italy (English) Italia (Italiano) Middle East & Africa Netherlands Netherlands (English) Nederland (Nederlands) Nordics Norway Poland Portugal Portugal (English) Portugal (Português) Romania Romania (English) Romania (Română) Russia Russia (English) Россия и СНГ (Русский) Slovakia Slovakia (English) Slovakia () Sweden Switzerland Switzerland (English) Switzerland (Deutsch) Turkey Turkey (English) Türkiye (Türkçe) Ukraine Ukraine (English) Україна (Українська) United Kingdom Asia Asia Pacific Australia and NZ 中国 India Indonesia 日本 대한민국 Malaysia Pakistan Philippines Singapore Sri Lanka Thailand Vietnam Home Careers Search Results Job Description Select a Topic See all jobs Our Company Life at IQVIA Clinical Research Associates AI & Machine Learning Talent Network Help create a healthier world. Start right here at IQVIA. Enter Keyword Enter Location Go Not ready to apply yet? Join our Talent Network. Senior Statistical Programmer Apply now Primary Location: Reading, Berkshire, United Kingdom Additonal Locations: Athens, Greece, GRC; Barcelona, Spain, ESP; Bucharest, Romania, ROU; Budapest, Hungary, HUN; Frankfurt, Germany, DEU; Milan, Italy, ITA; Vienna, Austria, AUT Full time R1154674 Date Posted: 10.09.2020 Job description We would expect form Senior Statistical Programmer to provide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs. 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.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 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.• Minimum of 5+ years of experience in Statistical Programming in pharmaceutical or medical devices industry• Good verbal and written communication skills. • Ability to work on multiple projects, plan, organize and prioritize activities. Required Knowledge, Skills andAbilities:• Experience as technical team lead directly engaging clients and coordinating tasks within a programming team• In-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 process• Advanced knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language • Should 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 skills• Ability to independently manage multiple tasks and projects • Ability to delegate work to other members of the SP team• Excellent accuracy and attention to detail• Ability to delegate work to other members of the SP team [SPM] • Exhibits routine and occasionally complex problem-solving skills• Ability to lead teams and projects and capable of managing at a group level• Recognizes 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.At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com. Apply now Save job Remove saved job 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 Let’s stay connected. Join our global Talent Network to receive alerts when new opportunities become available that match your career ambitions. Join our network Instagram YouTube Twitter LinkedIn Facebook Investors Customer Portal Careers News Events Contact Careers Sitemap Fraud alert Third-party access Suppliers Privacy Do not sell my personal information Terms of use COVID-19 resource center Fraud alert COVID-19 Candidate resource center © 2018-2020. All rights reserved. IQVIA® is a registered trademark of IQVIA Inc. in the United States, the European Union, and various other countries. Top of page
Please click here, if the job didn't load correctly.







Please wait. You are being redirected to the job in 3 seconds.