Job title: Lead Programmer
Company: GlaxoSmithKline Pte Ltd
Job description: Job Description : External: If you have strong ambition, solid technical skills and passion for innovation and global-working, and you want to make a difference to patients’ lives then you could be the future of GSK’s Quantitative Sciences India (
Job Description : External: If you have strong ambition, solid technical skills and passion for innovation and global-working, and you want to make a difference to 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 achieve 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. We have a number of ambitious goals to achieve in 2017, including a move to brand new state-of-the-art premises situated in the heart of Bangalore, and a significant expansion to grow the department. 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? Basic qualifications: Bachelors Degree in Engineering, Biotechnology, Computer Applicationsor related disciplines. More than 5 years experience in SAS programming (including SQL and SAS macro language) Recognized expertise in SAS programming and SAS macro code development. Effective written and verbal communication skills Excellent influencing skills, which are applied effectively at all levels of an organization and across multiple functions Strong time management skills; able to effectively organise and manage a variety of tasks across different projects Preferred qualifications: Good understanding 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 solid level of understanding of clinical trials, pharmaceutical regulatory and publishing processes (e.g. 21 CFR Part 11) Demonstrated knowledge of and experience in the application of CDISC data standards, primarily the creation and use of ADaM datasets. Ability to manage conflicting demands and priorities. Demonstrated ability to manage the outsourcing or externalization of statistical programming work in the clinical trials setting (e.g., working with CROs, academic institutions) Ability to develop creative solutions to applied problems. Ability to learn and apply advanced programming skills independently Responsibilities: Lead a small ( Plan, manage and execute programming activities across multiple studies, asset(s), indications or function to deliver all data analysis outputs to agreed timelines and quality, (e.g., macros, analysis datasets, pooled datasets, tables, figures and listings for regulatory submissions and publications). Oversee outsourced tasks to third party vendors and ensure their performance meets the agreed timelines, quality and budget requirements established for the project or study. Define, develop and embed 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 documents at the project level (e.g. submission documents, clinical report and publication). May author or co-author reporting analysis plans and department level documents (e.g. SOPs, working practice document). Develop broader technical knowledge and expertise (e.g. UNIX scripting, computing environments). Act as key statistical programming contact for study related stakeholders and provide solutions to complex problems. Manage stakeholders both internal and external. Develop broader technical knowledge and expertise (e.g. SAS Graphs, SAS Macros etc). Support future direction/wider objectives of project or business. Provide mentoring, training, development and performance feedback. Identify recurring problems and work with colleagues to initiate process improvement Our goalis to be one of the world’s most innovative, best performing and trusted healthcare companies. We believe that we all bring something unique to GSK and when we combine our knowledge, experiences and styles together, the impact is incredible. Come join our adventure at GSK where you will be inspired to do your best work for our patients and consumers. A place where you can be you, feel good and keep growing. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK’s commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. 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Location: Hyderabad, Telangana – Secunderabad, Telangana
Job date: Fri, 16 Apr 2021 22:38:28 GMT
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