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GlaxoSmithKline Pharmaceuticals
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41 GlaxoSmithKline Pharmaceuticals Jobs
Senior Programmer
5-7 years
Bangalore / Bengaluru
1 vacancy
Senior Programmer
GlaxoSmithKline Pharmaceuticals
posted 3d ago
Job Role Insights
Flexible timing
Key skills for the job
Job Description
- Bachelor s degree in engineering, Biotechnology, Computer Applications or related disciplines
- Minimum 1 year of experience in R programming.
- Biomarker Data Analysis background is 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.
- Knowledge of other SAS modules (e.g. SAS/GRAPH, SAS Output Delivery System).
- Knowledge of non-SAS programming packages/languages (Python, AI/ML).
- 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).
- 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).
- Provide technical advice, mentoring and training as relevant.
- The Senior 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.
Important notice to Employment businesses/ Agencies
Employment Type: Full Time, Permanent
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Anonymous · Research & Development
in Bangalore / Bengaluru
Work and opportunities
- Skill development - Good
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