Statistical Programmer @ Trigent

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Statistical Programmer

Trigent
3 - 8 years
Bengaluru
4 months ago
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Job Description

Role: Statistical Programmer

Location: Bengaluru(Hybrid)

Experience Level: 3+ Years

Employment Type: Full-time

Job Description

We are looking for an experienced Statistical Programmer with strong expertise in SAS programming and clinical trial data standards. The ideal candidate will have hands-on experience with CDISC (SDTM & ADaM) / OMOP mappings, regulatory documentation, and generation of submission-ready deliverables.

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 na****b@tr****t.com

Job Classification

Industry: Clinical Research / Contract Research
Functional Area / Department: Healthcare & Life Sciences
Role Category: Healthcare & Life Sciences - Other
Role: Healthcare & Life Sciences - Other
Employement Type: Full time

Contact Details:

Company: Trigent
Location(s): Bengaluru

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Desired Industry (*):

Functional area / Department (*):

Enter Skills (key skills, subjects, technologies & roles to use in search)

Write briefly about yourself, your experience and education (*)

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Please, check the file size and type.

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Home > Healthcare & Life Sciences - Other