Location: Bangalore, India
Job Type: Full-Time
Experience Required: Minimum 3+ Years Experience (Freshers Not Eligible)
Application Deadline: May 31, 2026
About the Role
A leading global clinical research and healthcare organization is hiring an experienced Statistical Programmer – RBQM Programming for its Bangalore location. This role is ideal for professionals with strong expertise in R programming, clinical trial data analysis, Risk-Based Quality Management (RBQM), and statistical programming within the pharmaceutical and CRO industry.
The selected candidate will work closely with cross-functional clinical research teams to develop robust programming solutions that enhance clinical trial quality, compliance, and data-driven decision-making.
Key Responsibilities
Develop, validate, and maintain R programs supporting Risk-Based Quality Management (RBQM) activities for clinical trial data
Collaborate with biostatistics, clinical data management, and clinical operations teams to understand project-specific data requirements
Perform statistical programming tasks for clinical trial reporting, data analysis, and visualization
Conduct quality checks and validation processes to ensure data accuracy, consistency, and regulatory compliance
Build and improve programming workflows, automation strategies, and R-based analytical processes
Support development of standardized programming methodologies and reusable R utilities
Create meaningful clinical data visualizations and analytical outputs for study teams and stakeholders
Required Qualifications
Bachelor’s degree in Statistics, Mathematics, Computer Science, Data Science, Biostatistics, or related quantitative field
Minimum 3 years of hands-on experience in R programming within the pharmaceutical, biotechnology, CRO, or clinical research industry
Strong expertise in R packages such as:
Tidyverse
ggplot2
survival
Experience handling and analyzing clinical trial datasets
Knowledge of industry-standard R frameworks and packages including:
ADMIRAL
OAK
Strong analytical thinking and problem-solving capabilities
Excellent communication and collaboration skills
Preferred Skills
Experience with SAS programming in clinical research environments
Familiarity with CRAN, POSIT, and open-source R repositories
Understanding of advanced clinical trial analytics and visualization methodologies
Exposure to regulatory and quality standards within clinical development programs
Why This Opportunity Matters
This role offers professionals an opportunity to work on advanced clinical trial analytics, RBQM frameworks, statistical programming, and data-driven quality management systems within the rapidly growing global pharmaceutical and CRO sector.
Professionals with expertise in R programming for clinical trials, biostatistics, data visualization, and RBQM programming are increasingly in demand across global healthcare and life sciences organizations.
Who Should Apply?
This opportunity is best suited for:
Statistical Programmers
Clinical SAS/R Programmers
Biostatistics Professionals
Clinical Data Science Specialists
RBQM Programming Experts
Freshers are currently not eligible for this position due to the required industry experience in clinical trial programming and R-based analytics.
Apply Now
Interested candidates can apply for this opportunity through the official company career portal before the application deadline.
For more verified global pharmaceutical, clinical research, pharmacovigilance, biostatistics, SAS programming, and data science jobs, visit ThePharmaDaily.com
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