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Sr. Statistical Programming Specialist

Fortrea
4+ years
Not Disclosed
Bangalore, India
2 May 21, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Sr. Statistical Programming Specialist

Company: Fortrea
Job Title: Sr. Statistical Programming Specialist
Job ID: 261989
Location: Bengaluru, Karnataka
Job Category: Biostatistics / Statistical Programming / Clinical Data Science
Employment Type: Full-time
Work Mode: Office / Home-Based (Hybrid)
Travel Requirement: Approx. 5%


Job Summary

Fortrea is hiring a Sr. Statistical Programming Specialist to lead statistical programming activities for clinical studies, develop CDISC-compliant datasets, generate analysis outputs, and support client deliverables in clinical research. This is an advanced programming role requiring strong SAS expertise and pharmaceutical/CRO industry experience.


Key Responsibilities

  • Lead statistical programming activities for clinical studies.

  • Act as Lead Statistical Programmer for assigned clinical pharmacology (CP) studies.

  • Plan, execute, and oversee:

    • Programming timelines

    • Resource estimation

    • Budget adherence

    • Quality deliverables

    • Cross-functional collaboration

    • Client interactions

  • Develop and maintain SAS programs for:

    • SDTM datasets

    • ADaM datasets

    • TFLs (Tables, Figures & Listings)

  • Perform Quality Control (QC) of:

    • SDTM

    • ADaM

    • TFL outputs

  • Generate submission documentation:

    • Define.XML

    • Define PDFs

    • Analysis Results Metadata (ARM)

    • Annotated eCRFs

    • Review Guides

  • Support specification development for:

    • SDTM

    • ADaM datasets

  • Review:

    • Statistical Analysis Plans (SAPs)

    • TFL shells

  • Support QA audits and client inspections.

  • Collaborate with programming, biostatistics, and project teams.


Required Qualifications

  • Bachelor’s Degree in:

    • Mathematics

    • Statistics

    • Computing

    • Life Sciences

    • Health Sciences

    • Related disciplines

Equivalent relevant experience may be considered.


Required Experience

  • 4+ years of SAS programming experience

  • Experience in:

    • CRO industry OR

    • Pharmaceutical industry

Strong experience in:

  • Clinical trial statistical programming

  • CDISC standards

  • Regulatory deliverables