- Bengaluru, India
Site Name: India - Karnataka - Bengaluru
Posted Date: Sep 6 2019
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?
- Bachelors Degree in Engineering, Biotechnology, Computer Applicationsor 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.
- 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
- Experience of the outsourcing or externalization of statistical programming work in the clinical trials setting (e.g., working with/for CROs, academic institutions)
The Associate Programmer acts as a support or lead programmer 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.
Our goal is 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.
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