Job Description

: Site Name: Hyderabad Wework Krishe Emerald Posted Date: Nov 1 2022 If you have strong ambition, solid technical skills, and passion for innovation and global-working, and you want to make a difference in patients' lives then you co

: Site Name: Hyderabad Wework Krishe Emerald Posted Date: Nov 1 2022 If you have strong ambition, solid technical skills, and passion for innovation and global-working, and you want to make a difference in patients' lives then you could be the future of GSK's Quantitative Sciences India (QSI) department, based in Bangalore. We are GlaxoSmithKline Asia Pvt Ltd, a world-leading Healthcare company with a mission to help people Do more, Feel better, Live longer. More than a billion patients use our products every day and we improve hundreds of millions of lives through the Sustainable Living Plan. Our Statisticians and Programmers belong to an established and large department of GSK that has built a strong reputation over its almost 20 year's heritage. With strong leadership, rich talent, and high energy levels, our staff achieves their goals both professionally and personally. They play key roles on therapeutically aligned, cross-functional, and global teams, supporting the design, analysis, and reporting of clinical trials. The roles are diverse, exciting, and rewarding and training opportunities are plentiful. There are even possibilities for International travel. Our greatest assets are our people so read on to find out more information about the range of exciting career opportunities currently available for Statisticians and Programmers with differing levels of experience, from new graduate to senior and managerial level roles. Are you the new talent that we're looking for Are you the future of GSK The Senior Programmer acts as a support for GSK clinical trials, accountable for creating, verifying, and documenting analyses of clinical data while adhering to study protocols, analysis plans, and GSK / industry standards. Responsibilities: Plan and manage programming activities across multiple studies to deliver all data analysis outputs to agreed timelines and quality, (e.g., analysis datasets, tables, figures, and listings for regulatory submissions and publications). Oversee outsourced tasks to third-party vendors to meet the agreed timelines, quality, and budget requirements established for the project or study. Implement data standards within a function, or therapeutic area in accordance with industry standards Responsible for programming and QC across a study/asset including submission activities adhering to relevant SOPs /policies. Participate in the design of other study delivery components (e.g. case report forms, study databases). Review and input into key study documents (e.g. SAP, CRF, etc.). Develop broader technical knowledge and expertise (e.g. UNIX scripting, computing environments). Provide technical advice, mentoring, and training as relevant. Identify recurring problems and work with colleagues to initiate process improvement Basic qualifications: Bachelor's Degree in engineering, Biotechnology, Computer Applications, or related disciplines Having a work experience of 4-6 Years More than 2 years' experience in SAS programming (including SQL and SAS macro language) Proficient in SAS programming and SAS macro code development. Effective written and verbal communication skills. Preferred qualifications: Knowledge of other SAS modules (e.g. SAS/GRAPH, SAS Output Delivery System). Knowledge of non-SAS programming packages/languages (e.g. Spotfire, S-Plus, R) A good level of understanding of the pharmaceutical regulatory and reporting processes (e.g. 21 CFR Part 11). Working knowledge of CDISC data standards, primarily the creation and use of ADaM datasets Experience in interacting with clinical study team members Ability to learn and apply advanced programming skills independently Ability to manage conflicting demands and priorities Experience of the outsourcing or externalization of statistical programming work in the clinical trials setting (e.g., working with/for CROs, academic institutions GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. Our success absolutely depends on our people. 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