Job Description

Job Title / Primary Skill: SAS Programmer

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Experience: 4 to 10 years

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Location: Across PAN India

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Looking for immediate to shorter notice period.

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Job Description Summary:

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Key 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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Required Qualifications: -

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- Strong 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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Preferred 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 environments.
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Desired 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 (India)
🏢 Iqvia
📍 India