Principal Clinical Programmer - US - Upper Providence
Location:
, Pennsylvania
Posted:
January 20, 2018
Reference:
166949
Why You?

Basic qualifications:
• BSc or higher in mathematics, statistics, computer science or related discipline

Preferred qualifications:
• Recognized expertise in SAS programming and SAS macro code development. Understanding of other SAS products (e.g. SAS/GRAPH, SAS Output Delivery System)
• A solid level of understanding of the pharmaceutical regulatory and publishing processes (e.g. 21 CFR Part 11
• Demonstrated knowledge of and experience in the application of CDISC data and standards, primarily the creation and use of ADaM datasets
• Knowledge of basic computer skills (MS Word, Excel, PowerPoint, Outlook)
• Knowledge of non-SAS programming packages/languages (e.g. Spotfire, S-Plus, R)
• Ability to manage conflicting demands and priorities and to negotiate successfully
• Project management or relevant experience
• Demonstrated ability to manage the outsourcing or externalization of statistical programming work in the clinical trials setting (e.g., working with CROs, academic institutions)
• Effective written and verbal communication skills
• Demonstrated direct interaction with clinical study team members of a consistently successful nature.

Why GSK?:
At GSK, our mission is to improve the quality of human life by enabling people to do more, feel better and live longer. Our three world-leading businesses research and deliver innovative medicines, vaccines and consumer healthcare products. We need a talented and motivated workforce to deliver against our strategy. To achieve this, we strive to attract the best people and to create an environment that empowers and inspires.

Contact information:

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A little about us:
We are a science-led global healthcare company on a mission to help people to do more, feel better and live longer.

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