Job Description

Site Name: Bengaluru Luxor North Tower Posted Date: Jun 13 2023 The Associate 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 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 of interacting with clinical study team members Ability to learn and apply advanced programming skills independently Ability to manage conflicting demands and priorities Summary: Job Category - Programming: Provides statistical programming expertise in support of discovery (e.g. Product Development, Investigational Material Supply, Safety Assessment and Drug Metabolism and Pharmacokinetics) and clinical development (e.g. analysis and reporting of Human Subject Research). Job Family - Data Use & Analytics: Develop, drive implementation and utilise methods, processes and systems to analyze data so that information is consumable for business use. Job Family Group - Digital, Data & Analytics: A set of tools and a mindset underpinned by advances in software, the increasing volumes of both structured and unstructured information and the ability to make sense of this data to identify trends and insights which allows us to engage with patients, customers and employees and drive better business decisions. 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 positively impact the health of 2.5 billion people by the end of 2030. Our success absolutely depends on our people. 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