SAS Programmer

IQVIA India; India; On-site; INR 800,000 - 1,200,000; Full time

Job summary

IQVIA India is seeking an experienced Clinical SAS Programmer to develop and validate programs for study deliverables. The role includes generating DVLs and supporting clinical outputs, with a focus on data accuracy and process quality.

You will collaborate with Data Management, Biostatistics, and Clinical Operations, using SAS macros and SQL to streamline workflows and ensure regulatory compliance.

Qualifications

• Strong proficiency in SAS programming for clinical data.
• Experience developing and reviewing Data Validation Listings (DVLs).
• Understanding of clinical trial data and programming standards.
• Working knowledge of SAS Macros and SQL.
• Strong analytical, problem-solving, and communication skills.
• Knowledge of programming best practices and quality standards.

Responsibilities

• Develop, validate, and maintain SAS programs for study deliverables.
• Generate and review DVLs to ensure data accuracy and consistency.
• Support creation of clinical data outputs, reports, and listings.
• Apply programming best practices, documentation, and QC.
• Collaborate with Data Management, Biostatistics, Clinical Ops.
• Use SAS macros and SQL to automate processes.
• Participate in data review and issue resolution.
• Support study milestones while adhering to regulatory standards.

Skills

SAS programming

DVL development

Data validation

Clinical data understanding

Problem-solving

Communication

Education

Bachelor's degree in Life Sciences / IT / Biostatistics

Tools

SAS

SQL

Power BI

Job description

Primary Skill: Clinical SAS, Edit checks, reconciliation, patient profile generation etc.

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