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Data Management Sas Programmer

Iqvia
IQVIA
1 years
Not Disclosed
Bengaluru, India
10 Feb. 20, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Data Management SAS Programmer

Location: Bengaluru, India
Job Type: Full-Time
Work Mode: Hybrid
Job ID: R1473762

Company Overview
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The organization accelerates the development and commercialization of innovative medical treatments to improve patient outcomes and global population health.

Job Summary
IQVIA is seeking a skilled Data Management SAS Programmer to support clinical database design, programming, and reporting activities within the clinical and healthcare domain. The selected candidate will work under guidance to assist with database modifications, SAS programming, clinical data processing, and report generation while ensuring compliance with project requirements and system capabilities.

This role is ideal for professionals with strong SAS programming expertise and foundational experience in clinical data management.

Key Responsibilities

  • Assist in database design and modifications to resolve database processing challenges.

  • Perform Edit Check Listings programming using SAS.

  • Execute Data Import Programming using SAS and SAS Output Delivery System (ODS) to generate RTF, PDF, and HTML reports.

  • Handle missing values, read raw data files, create data structures, and manage programming errors.

  • Access, manage, append, and concatenate SAS datasets efficiently.

  • Generate comprehensive reports using PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE, and PROC SQL.

  • Develop and utilize SAS Macros and SQL programming techniques.

  • Create SAS datasets from raw clinical data, including status and efficacy datasets.

  • Develop project-specific macros and formats.

  • Import vendor data and client data from external platforms.

  • Create custom listings and reports as per client requirements.

  • Write code using Base SAS programs, SAS procedures, and standardized macros.

  • Collaborate effectively within cross-functional teams.

Required Technical Skills

  • Strong knowledge of SAS/Base, Advanced SAS, SAS Macros, SAS/SQL, and SAS Grid.

  • Experience in clinical data management and clinical trial phases.

  • Proficiency in clinical/healthcare domain programming.

  • Knowledge of vendor import programming processes.

  • Strong analytical and problem-solving abilities.

  • Good communication and teamwork skills.

Education Requirements

  • Bachelor’s Degree in Computer Science, Life Sciences, Statistics, or a related field (or equivalent professional experience).

Experience Required

  • Minimum 1 year of experience in database administration or SAS programming within the clinical or healthcare domain.

Core Competencies

  • Clinical data processing and reporting

  • Statistical programming using SAS

  • Database management and validation

  • Report generation and clinical listings

  • Cross-functional collaboration

Why Join IQVIA
IQVIA offers opportunities to work on global clinical research projects, contribute to healthcare innovation, and build a strong career in clinical data management and SAS programming within a dynamic, growth-driven environment.

IQVIA maintains a strict zero-tolerance policy for candidate fraud and requires complete accuracy and integrity throughout the recruitment process.