Prin Stat Programmer

IQVIA LLC; Bengaluru; On-site; INR 3,500,000 - 5,500,000; Full time

Job summary

IQVIA LLC in Bengaluru, India, seeks a Principal Stat Programmer to lead SAS programming for clinical projects, ensuring SDTM/ADaM standards and regulatory readiness. You will develop and validate complex datasets, write ADaM specifications, and contribute to ADRG/Define.xml artifacts.

You will mentor junior staff, promote best practices, and collaborate with cross-functional teams to improve programming workflows and data quality across studies.

Qualifications

• Bachelor’s degree in Statistics, Computer Science or a related field.
• Master’s degree preferred in Statistics or Computer Science.

Responsibilities

• Develops and validates complex datasets and outputs using SAS per CDISC ADaM/SDTM requirements.
• Performs safety and/or efficacy analysis programming with efficacy datasets and outputs (Tables, Listings, Figures).
• Authors ADaM specifications for safety and/or efficacy analyses.
• Prepares regulatory submission documents including ADRG and Define.xml.
• Uses Pinnacle 21 for dataset validation and submission readiness.
• Mentors junior programmers and drives process improvements in workflows.

Skills

SAS programming

CDISC ADaM/SDTM

R programming

Mentoring

Leadership

Data analysis

Regulatory submissions

Problem solving

Communication

Quality assurance

Education

Bachelor's in Statistics/Computer Science

Master's in Statistics/CS (preferred)

Tools

SAS

R

Pinnacle 21 (P21)

Define.xml

Job description

The Principal Stat Programmer plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. This position demands proficiency in SAS programming and familiarity with CDISC standards, particularly ADaM and SDTM models. The role re quires experience in Safety and/or Efficacy analysis programming, including creation of efficacy datasets and efficacy outputs, ADaM specifications writing, and regulatory submission documentation. Key responsibilities include developing and validating complex data sets and outputs, collab orating with cross-functional teams to optimize processes, and providing technical guidance on statistical methodologies and programming best practices. The role also involves mentoring junior programmers and contributing to the continuous improvement of programming workflows and standards, supporting the overall quality deliverables of the statistical programming department.

Essential Functions

• Develops and validates complex datasets and outputs using SAS programming, ensuring compliance with CDISC standards such as ADaM and SDTM models.
• Performs Safety and/or Efficacy analysis programming, including creation of efficacy datasets and efficacy outputs (Tables, Listings, and Figures).
• Authors and reviews ADaM specifications for Safety and/or Efficacy analyses in compliance with CDISC standards.
• Creates and maintains regulatory submission documentation including Analysis Data Reviewer’s Guide (ADRG) and Define.xml.
• Utilizes Pinnacle 21 (P21) to validate datasets and ensure submission readiness and compliance with regulatory requirements.
• Collaborates with cross-functional teams to optimize statistical programming processes and enhance overall efficiency and accuracy.
• Provides technical guidance and expertise on statistical methodologies to support clinical trial projects and departments.
• Mentors and guides junior programmers, fostering their growth and development.
• Contributes to the continuous improvement of programming workflows and departmental standards.
• Ensures high-quality deliverables from the statistical programming department by adhering to best practices and established protocols.
• Leads initiatives to enhance programming tools and techniques, driving innovation in statistical programming.
• Partners with leadership to align programming objectives with larger organizational goals.
• Utilizes R programming to support statistical analyses, automation, data manipulation, reporting, and development of programming solutions where applicable.
• Minimum 1 year of hands‑on R programming experience is mandatory.
• Experience in Safety OR Efficacy analysis programming is required.
• Hands‑on experience in creation of efficacy datasets and efficacy outputs (Tables, Listings, and Figures).
• Experience in ADaM specifications writing for Safety and/or Efficacy studies.
• Experience in creating Analysis Data Reviewer’s Guide (ADRG), Define.xml, and performing dataset validation using Pinnacle 21 (P21).

Qualifications

• Bachelor's Degree Statistics, Computer Science or related field Req
• Master's Degree Statistics or Computer Science Pref.
• Strong knowledge of CDISC SDTM and ADaM standards.
• Ability to lead/manage others Capably leads and manages programming teams, ensuring adherence to standards and mentoring junior programmers.
• Demonstrated ability to maintain confidential information Maintains strict confidentiality of sensitive project data and internal communications.
• Demonstrates excellent judgment and decision‑making skills Exercises sound judgment and decision‑making in selecting statistical methods and programming techniques.
• Ability to work within tight timeframes and meet strict deadlines Effectively manages time and resources to deliver high‑quality programming outputs within tight deadlines.
• Project Demonstrated project management skills Executes projects efficiently, demonstrating strong project management skills to coordinate tasks and resources effectively.
• Possesses strong technical aptitude Demonstrates robust technical aptitude with a deep understanding of SAS programming and CDISC standards.
• Ability to analyze and interpret financial data Analyses and interprets financial data accurately to make informed decisions in statistical programming.
• Demonstrated analytical skills Utilizes strong analytical skills to assess statistical programming requirements and ensure data integrity.
• Demonstrated problem‑solving skills Applies effective problem‑solving skills to overcome programming challenges and optimize workflows.
• Excellent interpretation of complex statistical data Interprets complex statistical data with proficiency, ensuring accurate construction and validation of clinical datasets.
• Demonstrated written communication skills Exhibits strong written communication skills to document programming methodologies and procedures clearly.
• Strong verbal communication and listening skills Communicates effectively with cross‑functional teams to facilitate collaboration and improve statistical programming processes.
• Instills commitment to organizational goals Inspires and motivates programming teams to align their work with organizational goals and quality standards.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.