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    Novotech Hiring Pharmacy Graduates | Clinical Data Programmer Role

    Clinical Data Programmer Job at Novotech | Bangalore Opening

    A new opportunity is available for professionals interested in Clinical Data Programmer I (SDTM) jobs in Bangalore. This role focuses on transforming clinical trial data into standardized CDISC SDTM datasets using information from clinical protocols, eCRFs, and Statistical Analysis Plans (SAPs).

    About Novotech

    Novotech is a leading full-service contract research organization (CRO) specializing in the Asia-Pacific region. The company provides comprehensive clinical development services to the biotechnology and pharmaceutical industries, with a focus on delivering high-quality data and insights to support regulatory submissions and market access. Headquartered in Australia, Novotech operates across various locations, including Bangalore, India, to cater to the growing demand for clinical research services.

    Job Details

    • Position: Clinical Data Programmer I (SDTM)
    • Job Identification: 4176
    • Employment Type: Full-Time
    • Location: Bangalore, Karnataka, India
    • Workplace: Helios Business Park, Bangalore – 560103
    • Posting Date: August 28, 2026

    Clinical Data Programmer Job Description

    The Clinical Data Programmer I works closely with biostatisticians, statistical programmers, and other clinical project stakeholders to produce accurate, submission-ready SDTM outputs. The position may also support the preparation of clinical data submission packages for clients and regulatory authorities. This opportunity can be particularly relevant for candidates building a career in clinical data programming, SDTM programming, CDISC standards, and clinical research data management.

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    Key Responsibilities

    • Develop SDTM datasets based on clinical study protocols, eCRFs, and Statistical Analysis Plans.
    • Perform clinical data programming according to applicable CDISC SDTM standards.
    • Review clinical trial specifications and translate study requirements into standardized datasets.
    • Produce high-quality SDTM outputs for clinical studies.
    • Support preparation of data submission packages for clients and regulatory authorities.
    • Perform programming checks and quality-control activities to maintain data accuracy and consistency.
    • Work collaboratively with project biostatisticians and Statistical Programmers.
    • Coordinate with clinical and project stakeholders to resolve data or programming-related issues.
    • Ensure SDTM deliverables comply with study requirements and applicable data standards.
    • Support timely delivery of clinical programming milestones and submission-ready datasets.

    Eligibility Criteria

    The provided job description does not specify an exact educational qualification. Candidates with relevant life-science, pharmacy, statistics, computer science, or clinical research backgrounds may be considered depending on the employer’s screening requirements. Relevant qualifications may include B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc in Life Sciences, Biotechnology, Biostatistics, Statistics, Clinical Research, Computer Science, Bioinformatics, or related disciplines.

    Required Skills

    • CDISC SDTM
    • Clinical data programming
    • SDTM dataset development
    • SAS programming
    • Clinical trial data
    • eCRF/CRF interpretation
    • Clinical study protocols
    • Statistical Analysis Plans (SAP)
    • Data validation and quality control
    • Regulatory data submissions
    • Clinical database concepts
    • CDISC terminology
    • Documentation and specification review

    How to Apply?

    Application Link

    Why Consider This Opportunity?

    The Clinical Data Programmer I role provides exposure to an important part of the clinical development lifecycle. Professionals working in SDTM programming help convert clinical trial data into standardized structures that can support statistical programming, analysis, and regulatory submissions. Potential professional benefits include hands-on exposure to SDTM programming and clinical trial datasets, opportunities to develop expertise in CDISC standards, collaboration with biostatisticians and Statistical Programmers, and career development opportunities within clinical programming, statistical programming, and clinical data sciences.

    Qualified candidates are encouraged to apply for this opportunity at Novotech before the deadline. This role presents a significant chance to contribute to the clinical research field and develop a rewarding career in a Clinical Data Programmer role.

    CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE

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