R Programmer

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