Job Title / Primary Skill: SAS Programmer

nExperience : 4 to 10 years

nLocation : Across PAN India

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nLooking for immediate to shorter notice period.

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n Summary:

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nKey Responsibilities: -

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Develop, validate, and maintain SAS programs for clinical study deliverables.
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Generate and review Data Validation Listings (DVLs) to ensure data accuracy, completeness, and consistency.
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Support the creation and maintenance of clinical data outputs, reports, and listings.
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Apply programming best practices, including code optimization, documentation, and quality control.
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Collaborate with cross-functional teams including Data Management, Biostatistics, and Clinical Operations.
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Utilize SAS macros and SQL programming to automate and streamline processes.
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Participate in data review activities and contribute to issue resolution.
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Support study milestones and timelines while ensuring adherence to regulatory and company standards.
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nRequired Qualifications: -

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Solid proficiency in SAS programming.
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Hands-on experience in developing and reviewing Data Validation Listings.
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Good understanding of clinical trial data and programming standards.
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Working knowledge of SAS Macros and SQL.
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Solid analytical, problem-solving, and communication skills.
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Demonstrated understanding of programming best practices and quality standards.
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nPreferred Qualifications: -

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Experience with Protocol Deviation Listings and Patient Profile generation.
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Knowledge of the Clinical Data Management (CDM) full lifecycle.
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Exposure to Power BI for data visualization and reporting.
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Experience working in regulated clinical research settings.
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nDesired Skills: -

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Clinical Data Programming
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SAS Base, SAS Macros, SQL
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Data Validation & Quality Control
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Protocol Deviations
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Patient Profiles
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Clinical Data Management (CDM)
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Power BI (Preferred)
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Team Collaboration & Stakeholder Communication
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📌 Sas Programmer Mysuru
🏢 Iqvia
📍 Mysuru