Bengaluru Karnataka Clinical sas programmer Jobs – 27 Open Jobs Today

Statistical Programmer Sr
eClinical Solutions —Bengaluru, Karnataka
- Remote
- Computer science
- B.Sc
- Master's degree
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Lead Biostatistician
Cepheid —Bengaluru, Karnataka
- Full-time
- Doctoral degree
- Master's degree
- Machine learning
- Paid time off
Sr Clinical Data Scientist
Novo Nordisk —Bengaluru, Karnataka
- English
- Master's degree
- Analysis skills
9d
Senior/ Principal Statistical Programmer | Long Term Contract | Remote
Two95 International Inc. —Bengaluru, Karnataka
- Remote
- SQL
- Python
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Prin Stat Programmer
IQVIA —Bengaluru, Karnataka
- Full-time
- Remote
- Computer Science
- Master's degree
- Analysis skills
- Work from home
Sr. Stat Programmer
IQVIA —Bengaluru, Karnataka
- Full-time
- Remote
- Computer Science
- English
- Master's degree
- Work from home
Director of Biometrics Automation & AI Architecture
Quanticate —Bengaluru, Karnataka
- Full-time
- Hybrid work
- Research
- Master's degree
- AI
- Health insurance
- Paid time off
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Statistical Programmer Sr

eClinical Solutions -
Bengaluru, Karnataka

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Job details

Qualifications

Statistics
Computer science
Statistics
XML
SAS
Relational databases
B.Sc
R
Git
Master's degree
Databases
SQL
Science
Bachelor's degree
Macros
Clinical trials
GitHub
AI
GitLab
Communication skills
Shell Scripting
FDA regulations
SDLC

Full job description

OVERVIEW

Experienced Statistical Programmer with expertise in supporting multiple clinical studies through the development, validation, and delivery of high-quality statistical programming outputs. Proficient in SAS (Base SAS, SAS/STAT, and Macro Language) and CDISC standards, including SDTM, ADaM, and TLF development for regulatory submissions. Skilled in creating analysis datasets, safety and efficacy tables, listings, figures, Define.xml, and submission packages compliant with FDA, PMDA, and EMA requirements. Strong knowledge of the clinical drug development process, data automation, safety reporting, DSUR/PSUR deliverables, and Pinnacle 21 validation. Proven ability to collaborate with internal stakeholders, proactively resolve programming issues, and ensure timely, compliant, and accurate study deliverables. Use of R and AI tools to augment, enhance day to day programming is a huge plus.

KEY TASKS & RESPONSIBILITIES

➢ Led multiple studies on end-to-end programming while serving as the primary point of contact for clients.

➢ Develop specifications and SAS programs for SDTM datasets and clinical data analysis deliverables.

➢ Create specifications and SAS programs for ADaM datasets supporting trial-level reporting and integrated safety and efficacy analyses.

➢ Develop, maintain, and validate Tables, Listings, and Graphs (TLGs) based on biostatistical requirements and Statistical Analysis Plans (SAPs).

➢ Program and QC data listings, summaries, graphs, and statistical models as required.

➢ Design and maintain reusable SAS macros to support Phase I–IV clinical trial reporting.

➢ Generate submission-ready datasets and output using industry standards, SDLC practices, and regulatory requirements.

➢ Collaborate with cross-functional teams to ensure timely delivery of high-quality study outputs.

➢ Maintain project documentation in compliance with SOPs, processes, and quality standards.

➢ Ensure adherence to eClinical Solutions and industry guidelines, procedures, and regulatory expectations.

➢ Ability to independently write R programs and convert SAS programs to R programs using AI tools to create datasets and TLFs.

Education & Experience

➢ Basic Science/Bachelor of Science degree (Master in Statistics or related science preferred) in health-related fields, computer science or equivalent experience preferred.
➢ SAS Certified
➢ R programming experience is a plus
➢ Knowledge and experience in using AI to gain programming efficiencies is a plus

Professional Skills

➢ Minimum 8+ years in Pharmaceutical/Biotechnology industry or equivalent IT consulting role preferred.
➢ Strong experience in preparations for NDA filings
➢ Strong knowledge of E6, E3, E9 guidelines, 21 CFR Part 11 and clinical trial methodologies
➢ Knowledge of coding dictionaries (WHO, COSTART, ICD-9, MedDRA)
➢ Knowledge of CDISC® related data models like SDTM, and ADAM.
➢ Experience of working on multiple clinical protocols at the same time.
➢ Excellent verbal and written communication skills
➢ Detail oriented, ability to multitask with strong prioritization, planning and organization skills.
➢ Excellent team player

Technical Skills

➢ Advanced SAS programming expertise in data extraction, integration, analysis, reporting, and automation.
➢ Proficient in Base SAS, PROC SQL, Macro Programming, ODS, SAS/GRAPH, SAS/STAT, SAS/CONNECT, and SAS/ACCESS.
➢ Extensive experience with SAS reporting procedures, including PROC SQL, PROC REPORT, PROC SUMMARY / PROC Means, PROC FREQ, and PROC TRANSPOSE, in clinical research environments.
➢ Skilled in working with relational databases, SAS performance optimization, and process automation through batch, shell scripting and AI tools.
➢ Experienced in R programming (tidyverse, dplyr, admiral, rtables ggplot2, xportr, flextable) and Git-based version control (GitHub, GitLab).
➢ Experienced in developing Tables, Listings, and Graphs (TLGs) using SAS and R for clinical trial analysis and reporting.

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Refine Your Search

clinical sas programmer jobs in bengaluru karnataka

Statistical Programmer Sr

Lead Biostatistician

Sr Clinical Data Scientist

Senior/ Principal Statistical Programmer | Long Term Contract | Remote

Prin Stat Programmer

Sr. Stat Programmer

Director of Biometrics Automation & AI Architecture

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