SAS PROGRAMMER

IQVIA; India; On-site; INR 800,000 - 1,600,000; Full time

Job summary

IQVIA is seeking an experienced SAS Programmer to develop, validate, and maintain SAS programs for clinical study deliverables. You will generate and review Data Validation Listings (DVLs) to ensure data accuracy and consistency, and support the creation of clinical data outputs and reports.

The role requires hands-on SAS programming, SAS macros, and SQL knowledge, with collaboration across Data Management, Biostatistics, and Clinical Operations to meet milestones and regulatory standards.

Qualifications

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

Responsibilities

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

Skills

SAS programming

SAS Macros

SQL

Analytical skills

Communication skills

Tools

Power BI

Job description

Job Title / Primary Skill: SAS Programmer

Experience : 4 to 10 years

Location : Across PAN India

Looking for immediate to shorter notice period.

Job Description Summary:

Key Responsibilities: -

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

Required Qualifications: -

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

Preferred Qualifications: -

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

Desired Skills: -

• Clinical Data Programming
• Data Validation & Quality Control
• Protocol Deviations
• Clinical Data Management (CDM)
• Power BI (Preferred)
• Team Collaboration & Stakeholder Communication