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Senior Programmer

5.-7 years
Not Disclosed
10 March 19, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Tech/BCS/BCA Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.