Location: Kochi, India / Kolkata, West Bengal, India
Company: IQVIA
Job ID: R1538459
Employment Type: Full-Time
Application Deadline: April 29, 2026
Experience Required: 1–2 years (Not suitable for freshers)
About the Company
IQVIA is a globally recognized leader in clinical research services, healthcare analytics, and commercial insights. The organization leverages advanced data science and technology to accelerate drug development, improve patient outcomes, and drive innovation across the life sciences industry.
Job Overview
The India Statistical Programmer role is a critical position within clinical research and biostatistics, responsible for developing, validating, and managing statistical programming deliverables. This role supports clinical trials by generating high-quality datasets, tables, listings, and figures (TLFs), ensuring compliance with regulatory standards and study protocols.
Key Responsibilities
Perform and plan programming, testing, and documentation for statistical outputs including tables, listings, and figures (TLFs)
Develop and validate analysis datasets (ADaM/SDTM) and manage data transfers for internal and external stakeholders
Execute database integration across multiple studies and data sources
Create detailed programming documentation including specifications and development plans
Provide technical expertise and contribute to problem-solving across cross-functional teams
Develop, implement, and validate macros, tools, and automation processes to enhance efficiency
Support statistical team lead activities for single-study projects under supervision
Manage scope of work, timelines, and deliverables while identifying out-of-scope tasks
Contribute to budget estimation, resource planning, and forecasting for assigned studies
Train and mentor junior programmers and new team members
Required Qualifications
Master’s Degree in Computer Science, Statistics, or related field with minimum 1 year of relevant experience
OR
Bachelor’s Degree in Computer Science, Statistics, or related field with minimum 2 years of relevant experience
Equivalent combination of education and experience may be considered
Strong knowledge of statistical concepts, clinical trial processes, and drug development lifecycle
Hands-on experience with SAS programming including Base SAS, SAS/STAT, and SAS Macro Language
Excellent analytical, organizational, and problem-solving skills
Strong communication and stakeholder management abilities
High attention to detail and accuracy in data handling
Ability to manage multiple projects and meet deadlines efficiently
Preferred Skills
Experience with CDISC standards (SDTM, ADaM)
Understanding of regulatory guidelines including ICH-GCP
Exposure to clinical data management and biostatistics workflows
Why Join IQVIA
Work with a globally leading CRO and healthcare intelligence organization
Gain exposure to international clinical trials and regulatory environments
Opportunity to build expertise in statistical programming and clinical data science
Collaborative, innovation-driven, and growth-focused work culture
Important Note for Applicants
This position requires prior experience in statistical programming or clinical data analysis. Freshers are advised to apply for entry-level roles such as SAS Programmer Trainee, Clinical Data Analyst, or Biostatistics Intern roles before progressing to this position.
Application Process & Compliance
IQVIA follows a strict zero-tolerance policy toward recruitment fraud. All applicants must ensure that the information provided during the hiring process is accurate and complete. Any discrepancies may lead to disqualification or termination as per applicable regulations.
How to Apply
Apply through the official careers portal of IQVIA or explore verified global opportunities on ThePharmaDaily.com, your trusted platform for pharma, clinical research, and pharmacovigilance careers.
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