🏷️ Job Title
Statistical Programmer
Job ID: R1438804
Location: Thāne, India (Home-based | Additional locations available)
Job Type: Full-Time
🔗 Apply Now | Save Job | Share: Email | LinkedIn | Facebook
🧭 Job Overview
The Statistical Programmer is responsible for creating and validating SAS programs to generate derived analysis datasets and outputs such as tables, listings, and figures. This role provides programming support to project teams, ensures adherence to standards and regulatory requirements, collaborates with internal and external stakeholders, and identifies opportunities to improve efficiency in programming processes.
🔑 Key Responsibilities
Programming & Validation
Develop SAS programs for derived analysis datasets and content for tables, listings, and figures (TFLs).
Perform programming validation to ensure quality and accuracy of analysis datasets and outputs.
Independently lead or perform programming assignments with minimal supervision.
Project Support & Collaboration
Provide programming support to project teams including the development of strategies, standards, and specifications.
Review key planning documents (statistical analysis plan, data presentation plan, data review plan) to ensure alignment with programming objectives.
Assess impact of planning documents on programming activities.
Interact with vendors on programming standards, conventions, specifications, and file transfers.
Quality & Compliance
Ensure quality of Global Biometric and Data Sciences (GBDS) deliverables by applying standards and complying with regulatory and corporate SOPs.
Support electronic submission preparation and review processes.
Participate in improvement initiatives to enhance efficiency and consistency.
🎓 Minimum Requirements
Bachelor’s degree in Statistics, Biostatistics, Mathematics, Computer Science, or Life Sciences.
Minimum 3 years of programming experience in the industry (US military experience may be considered).
Proficiency in SAS, R, or other programming languages for producing derived analysis datasets and TFLs.
Understanding of clinical data structures, e.g., CDISC standards, relational databases.
Skills in software tools like MS Office, XML.
Experience handling upstream data (e.g., multiple data forms, eDC, SDTM) and producing outputs for downstream requirements (e.g., ADaM, Data Definition Table, e-submissions).
Knowledge of regulatory, industry, and technology standards and requirements.
Familiarity with statistical terminology, clinical tests, medical terminology, and protocol designs.
Ability to work effectively within clinical team environments.
🌟 Preferred Qualifications
3+ years of clinical/statistical programming experience within pharmaceutical clinical development.
Knowledge of drug development process, clinical trial methodology, statistics, and global regulatory requirements.
Experience with additional software packages (e.g., R).
Experience with Linux operating system.
🏢 About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We connect data, technology, and science to accelerate the development and commercialization of innovative medical treatments to improve patient outcomes worldwide.
Learn more at: https://jobs.iqvia.com
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