Statistical Programmer

3 - 8 years

15 - 20 Lacs

Posted:1 hour ago| Platform: Naukri logo

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Skills Required

Work Mode

Hybrid

Job Type

Full Time

Job Description

Role:

Location:

Experience Level:

Employment Type:

Statistical Programmer

Key Responsibilities

  • Develop and validate

    SAS programs

    for clinical trial datasets.
  • Map clinical data to

    CDISC standards (SDTM & ADaM)

    and/or

    OMOP

    .
  • Prepare and review

    CDISC documentation

    (define.xml, reviewers guide, aCRF).
  • Perform

    Pinnacle21 validation

    for submission readiness.
  • Produce

    TLFs (Tables, Listings, Figures)

    based on SAP requirements.
  • Ensure

    data quality and compliance

    with regulatory standards.

Must-Have Skills

  • 3+ years

    of experience as a Statistical Programmer.
  • Strong

    SAS programming

    expertise.
  • Solid understanding of

    clinical trial processes

    .
  • Hands-on experience with

    SDTM, ADaM, and OMOP

    .
  • Knowledge of

    CDISC documentation & Pinnacle21 validation

    .
  • Fluent in

    English

    , with strong

    problem-solving, communication, and detail orientation

    .

    Role & responsibilities

If you or someone you know fits this role, apply directly through the job post or share your resume at

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