Job Title / Primary Skill: SAS ProgrammerExperience : 4 to 10 yearsLocation : Across PAN IndiaLooking 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.Positive 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 ProgrammingSAS Base, SAS Macros, SQLData Validation & Quality ControlProtocol DeviationsPatient ProfilesClinical Data Management (CDM)Power BI (Preferred)Team Collaboration & Stakeholder Communication

📌 SAS PROGRAMMER (Mumbai)
🏢 Iqvia
📍 Mumbai