Senior Programmer
Location: Bengaluru, India
Department: Digital Data & Analytics
Job ID: 416253
Contract Type: Full Time
Posted Date: March 18, 2025
Years of Experience: 5.5 - 7+ years
Skill Set / Exposure:
Programming background, CDISC Standards, ADAM, TLF, R, SAS, and Biomarker Data Analysis preferred.
Work Location: Bengaluru
Job Description:
Basic Qualifications:
Bachelor’s degree in Engineering, Biotechnology, Computer Applications, or related disciplines.
Minimum 1 year of experience in R programming.
Background in Biomarker Data Analysis preferred.
4+ 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.
Preferred Qualifications:
Knowledge of other SAS modules (e.g., SAS/GRAPH, SAS Output Delivery System).
Knowledge of non-SAS programming languages (Python, AI/ML).
Understanding of 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 interacting with clinical study team members.
Ability to learn and apply advanced programming skills independently.
Ability to manage conflicting demands and priorities.
Experience outsourcing or externalizing statistical programming work in clinical trials (e.g., working with/for CROs, academic institutions).
Responsibilities:
Plan and manage programming activities across multiple studies to deliver 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 agreed timelines, quality, and budget requirements.
Implement data standards within a function or therapeutic area following 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 provide input on key study documents (e.g., SAP, CRF, etc.).
Provide technical advice, mentoring, and training as relevant.
Role Summary:
The Senior Programmer supports GSK clinical trials by creating, verifying, and documenting analyses of clinical data, adhering to study protocols, analysis plans, and GSK/industry standards.
Inclusion at GSK:
GSK is committed to fostering an inclusive environment. If you require any adjustments during the recruitment process, please contact the Recruitment Team at IN.recruitment-adjustments@gsk.com.
Why GSK?
GSK unites science, technology, and talent to get ahead of disease, positively impacting billions of lives while providing a thriving environment for employees.
Important Notice:
GSK does not charge any fees during the recruitment process. If you encounter suspicious job advertisements or emails not ending in "gsk.com," please contact askus@gsk.com to verify authenticity.
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