Title : Statistical Programmer 2 / Sr. Statistical Programmer United States / Nationwide - home or office based-1308004

Description     This is a home based opportunity anywhere in North America. The Clinical Development Services division of Quintiles has more depth of therapeutic expertise and a broader range of services than any other service provider. We conduct both US and Global trials in all therapeutic areas.  In fact, Quintiles conducts more clinical trials than anyone else in the world.  Become involved in work that improves the quality of life for people around the globe.  Let your career soar!  We are seeking an enthusiastic Statistical Programmer 2/Sr. Statistical Programmer who will provide advanced technical expertise to develop and maintain programs to meet internal and external clients' needs. Plan and lead the development of project-related solutions to the full scope of statistical programming tasks. Provide technical expertise to the Statistical Programming department. see  https://quintiles.taleo.net/careersection/10080/jobdetail.ftl RESPONSIBILITIES ·         Perform and plan: the programming, testing, and documentation of programs for use in creating statistical tables, figures and listing, the programming of analysis dataset (derived datasets) and transfer files for internal and external clients. and the programming  quality control checks for the source data and report the data issues periodically. ·         Detect errors in detail, corrects them (e.g., reviews tables/listings, edit checks output and SAS programs to ensure quality of deliverable) and report it to appropriate personals (internal or external clients) ·         Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department. ·         Perform and plan the development, implementation and validation of new process technologies, macros and applications. ·         Fulfill project responsibilities at the level of technical team lead for single studies, under supervision. ·         Understand timelines for and milestones affecting their work and alert supervisor to potential slippage. ·         Provide training and mentoring to SP team members Qualifications   REQUIRED    ·         Masters degree in computer science or related field and 1 year relevant experience; Bachelor's degree in computer science or related field and 3 years relevant experience; or equivalent combination of education, training and experience   ·         Knowledge of statistics, programming and/or clinical drug development     process ·         In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines   ·         Ability to implement programming  specifications, as appropriate ·         Ability to estimate programming scope of work and assist in communicating project status ·         Working knowledge of Base SAS, SAS/STAT, SAS Graph and SAS Macro Language ·         Familiarity with SAS Drug Development (SDD) and Clinical Data Integration (CDI) would be preferred • Familiarity with SAS Drug Development (SDD) and Clinical Data Integration (CDI) would be preferred • Good organizational, interpersonal, leadership, communication skills and multi-tasking abilities. Primary Location: USA-Kansas-Overland Park Organization: USA02 - US Clinical Development Svcs