Job Title
Statistical Programmer – RBQM Programming
Company
Fortrea
Location
Bangalore, India
Employment Type
Full-time
Job Overview
This role focuses on statistical programming in clinical trials, specifically supporting Risk-Based Quality Management (RBQM). You will develop and maintain R programming solutions to analyze clinical trial data, generate insights, and support quality and risk monitoring processes.
Key Responsibilities
1. Statistical Programming (R Language)
Develop and maintain R programs for RBQM in clinical trials
Work with clinical trial datasets using R
Implement data analysis and reporting solutions
2. Data Analysis & Visualization
Perform statistical analysis of clinical trial data
Create data visualizations using R tools
Support reporting for risk-based quality management
3. Cross-Functional Collaboration
Work with clinical operations, data management, and biostatistics teams
Understand project-specific data requirements
Translate business/clinical needs into programming outputs
4. Quality Control & Validation
Perform QC of statistical outputs
Ensure accuracy, consistency, and reproducibility of results
Validate programming outputs before delivery
5. Process Improvement
Contribute to improving programming standards
Support development of best practices in R programming
Enhance efficiency of RBQM processes
Required Qualifications
Bachelor’s degree in:
Statistics
Mathematics
Computer Science
Data Science
Or related quantitative field
Required Experience
Minimum 3 years experience in R programming
Experience working with clinical trial data
Required Skills
Technical Skills
Strong proficiency in R programming
Knowledge of R packages such as:
Tidyverse
ggplot2
survival
Experience in clinical trial data analysis
Data visualization skills
Understanding of RBQM concepts
Advanced/Industry Tools (Preferred)
ADaM/clinical programming frameworks
Industry packages like:
ADMIRAL
OAK
Familiarity with:
SAS programming
CRAN / Posit ecosystem
Core Competencies
Strong analytical thinking
Problem-solving ability
Attention to detail
Ability to work with complex datasets
Understanding of clinical research data
Soft Skills
Good communication skills
Team collaboration
Ability to interpret clinical requirements
Time management and delivery focus
Role Summary (Simple Explanation)
This is a clinical statistical programming role, where you will:
Use R programming to analyze clinical trial data
Build tools for risk monitoring in clinical studies (RBQM)
Create data visualizations and reports
Support quality control of clinical data outputs
Work with global clinical research teams
Key Insight
This is a mid-level technical role (3+ years experience)
Strong fit for candidates interested in:
Clinical data science
Biostatistics programming
R / SAS clinical analytics careers
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Remote, India | Siliguri |Illinois :
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