Senior Programmer - R

Ephicacy

India

On-site

INR 10,000,000 - 15,000,000

Full time

14 days+

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Job summary

A biotechnology research company is seeking an Associate Manager - HR in India. The role requires strong R programming skills and experience with clinical trial data to develop and maintain global datasets. Candidates should hold a bachelor's degree in a quantitative field and have at least 3 years of relevant experience. This position is full-time and involves collaboration with cross-functional teams to ensure compliance with industry standards and provide data analysis support.

Qualifications

  • Bachelor's degree in a quantitative field.
  • Minimum of 3 years of experience with R programming.
  • Familiarity with clinical trial data.

Responsibilities

  • Develop and maintain global R codebase for CDISC ADaM datasets.
  • Ensure compliance with industry standards.
  • Collaborate with cross-functional teams.

Skills

R programming
Data visualization techniques
Analytical skills
Communication and teamwork

Education

Bachelor's degree in a quantitative field

Tools

R (Tidyverse, ggplot2, survival)
CDISC ADaM and SDTM standards
ADMIRAL
OAK

Job description

Associate Manager - HR @ Ephicacy | India & North America

Qualifications

  • Bachelor's degree in a quantitative field (e.g., Statistics, Mathematics, Computer Science, Data Science)
  • Minimum of 3 years of experience in R programming including familiarity with R packages (e.g., Tidyverse, ggplot2, survival)
  • Familiarity with data visualization techniques and tools in R
  • Experience with clinical trial data and familiarity with CDISC ADaM and SDTM standards
  • Knowledge of industry R packages like ADMIRAL and OAK
  • Strong analytical and problem‑solving skills
  • Excellent communication and teamwork abilities

Role Responsibilities

  • Develop and maintain global R codebase for generating CDISC ADaM datasets and tables, listings, and figures in accordance with clinical trial data requirements
  • Ensure compliance with industry standards and regulatory requirements
  • Collaborate with cross‑functional teams to understand and implement project‑specific data needs
  • Provide technical expertise and support for data analysis and reporting tasks
  • Perform quality control and validation of outputs to ensure accuracy and consistency
  • Contribute to process improvements and development of programming standards using R

Seniority Level – Associate

Employment Type – Full‑time

Job Function – Other

Industries – Biotechnology Research and Pharmaceutical Manufacturing

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