Instagram
youtube
Facebook

Sr Statistical Programming Specialist (R Programming)

3+ years
Not Disclosed
10 June 11, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Summary

Fortrea is hiring a Sr Statistical Programming Specialist (R Programming) in Mumbai for its Clinical division. This role involves developing and maintaining R programs for clinical trial data analysis and reporting in compliance with industry and regulatory standards. Candidates with at least 3 years of R programming experience and a strong background in clinical trial data handling, CDISC ADaM, and SDTM are encouraged to apply. This is an On-site opportunity offering hands-on exposure to clinical data analysis and cross-functional collaboration in a global pharmaceutical setting.


Key Responsibilities

  • Develop and maintain R programs to generate CDISC SDTM and ADaM datasets, along with tables, listings, and figures.

  • Ensure programming outputs meet clinical trial data requirements, industry standards, and regulatory guidelines.

  • Collaborate with cross-functional teams to gather and implement project-specific data needs.

  • Provide technical expertise and support for clinical data analysis and reporting tasks.

  • Conduct quality control and validation to ensure data accuracy and consistency.


Required Skills & Qualifications

  • Bachelor's degree in Statistics, Mathematics, Computer Science, Data Science, or a related quantitative field.

  • Minimum 3 years of hands-on experience with R programming in the context of clinical trials.

  • Familiarity with R packages for data analysis, reporting, and visualization.

  • Experience working with clinical trial data, including knowledge of CDISC ADaM and SDTM standards.

  • Strong analytical and problem-solving abilities.

  • Effective communication skills and ability to work collaboratively in a team environment.


Desirable Skills

  • Knowledge of other open-source packages and tools.

  • Experience with SAS software for clinical data analysis.

  • Familiarity with CRAN, POSIT, and other open-source repositories.


Perks & Benefits

  • Competitive salary (not specified in the description)

  • Opportunities for professional growth and development

  • Exposure to global clinical data standards and regulatory practices

  • Collaborative work environment focused on innovation in drug development


Company Description

Fortrea is a global Contract Research Organization (CRO) delivering world-class clinical development, pharmacovigilance, and technology solutions across more than 20 therapeutic areas. Operating in approximately 100 countries, Fortrea is committed to transforming drug and device development for healthcare clients worldwide.


Work Mode

On-site – Mumbai


Call-to-Action

If you are an experienced statistical programmer passionate about advancing clinical research using R programming, apply now to join Fortrea's Clinical division in Mumbai and make a significant impact in global drug development.