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Senior Programmer Analyst II (Statistical programmer)

Fresher   Bangalore   07 Jul, 2026
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaEnvironmentOccupational Health / Safety
EmploymentTypeFull-time

Job Description

    We are seeking an experienced Statistical Programmer with 8 OR 8 years of experience in clinical trials and pharmaceutical research. The ideal candidate should possess strong expertise in SAS programming and clinical data standards, including SDTM, ADaM, and TFL development.Key Responsibilities:
    • Develop and validate SDTM and ADaM datasets as per CDISC standards.
    • Generate Tables, Listings, and Figures (TLF/TFL) for clinical study reports.
    • Perform SAS programming for clinical trial data analysis and reporting.
    • Collaborate with Biostatisticians, Data Management, and Clinical Operations teams.
    • Review protocol, SAP, CRF, and data specifications.
    • Ensure compliance with regulatory requirements and industry standards.
    • Perform quality checks and validation of programming outputs.
    • Support regulatory submissions and audits when required.
    Required Skills:
    • 8 years of Statistical Programming experience.
    • Strong SAS Programming skills.
    • Hands-on experience with SDTM, ADaM, and TFL/TLF development.
    • Knowledge of CDISC standards and clinical trial processes.
    • Experience in pharmaceutical, biotechnology, or CRO environments.
    • Exposure to regulatory submissions (FDA, EMA, PMDA) is preferred.
    • Strong analytical and problem-solving skills.

Keyskills :
clinicaladamsdtmprogrammingtrialspharmaceuticaltlftflcro.statisticalcdisc

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