R Programmer
2 weeks ago
Role **:R Programmer, India.**
Location : Remote (Any where in india)
Shift : Day Shift
**Job Summary**:
**Key Responsibilities**:
Develop, validate, and maintain R scripts and SAS programs for analyzing and reporting clinical trial data.
Work with CDISC standards (SDTM, ADaM) to generate regulatory submission datasets.
Create statistical analysis reports, TLFs, and ad-hoc analyses in both R and SAS.
Collaborate with biostatisticians, data managers, and clinical teams to ensure data integrity and accuracy.
Automate data analysis workflows and optimize existing R/SAS programs for efficiency.
Support regulatory submissions and responses to Health Authorities (e.g., FDA, EMA).
Perform quality control (QC) checks and debugging of R and SAS programs.
Document programming activities following GCP and SOPs to ensure compliance.
**Required Qualifications**:
Bachelor’s or Master’s degree in Statistics, Biostatistics, Computer Science, or a related field.
5+ years of experience in clinical trial data analysis using R and SAS.
Strong knowledge of CDISC (SDTM, ADaM) standards and regulatory requirements.
Experience in generating Tables, Listings, and Figures (TLFs) for clinical studies.
Proficiency in R Markdown, Shiny, ggplot2, tidyverse, and other R-based visualization tools.
Hands-on experience with SAS macros, PROC SQL, and statistical procedures.
Familiarity with clinical trial design, ICH-GCP guidelines, and regulatory submission processes.
Excellent problem-solving and debugging skills.
**Job Types**: Full-time, Permanent
Pay: ₹600,000.00 - ₹1,800,000.00 per year
**Benefits**:
- Paid sick time
- Provident Fund
Schedule:
- Day shift
- Monday to Friday
- Morning shift
**Experience**:
- R programming: 3 years (required)
- minimum R Programming experience?: 1 year (required)
- clinical trial data analysis: 1 year (required)
Work Location: Remote
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