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Post Name CLINICAL SAS PROGRAMMER
Qualification UG
Experience 4 – 9 Years
Opening date: 07/08/2019
Job Description: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 Experience of the outsourcing or externalization of statistical programming work in the clinical trials setting (e.g., working with/for CROs, academic institutions) The Senior 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.
Location Bengaluru
Openings 01
Salary Not Disclosed by Recruiter
Interview Time & Date & Recruiter Name Recruiter Name:HR Contact Company:GlaxoSmithKline Pharmaceuticals Limited
Email :shivalingappa.x.kotabagi@gsk.com
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