Database Management Analyst (Clinical SAS Programming)

About IQVIA

IQVIA is a global leader offering advanced analytics, technology solutions, and contract research for the life sciences sector. The company integrates human data science with expansive medicinal knowledge to transform clinical development and commercial strategies, accelerating healthcare innovations. Employing over 86,000 professionals globally, IQVIA operates across 100+ countries and was recognized in FORTUNE's 2023 "World's Most Admired Companies." The organization fosters career growth while impacting health outcomes worldwide.

Role Overview

This role involves supporting clinical data management within biometrics through programming and quality assurance. It requires close collaboration with multidisciplinary teams to deliver precise, quality clinical data and reports, adhering strictly to study timelines and regulatory guidelines.

Key Responsibilities

• Provide programming support for clinical data management activities in the biometrics domain.
• Engage with programmers, data managers, statisticians, safety, regulatory personnel, and project teams to maintain data integrity.
• Ensure clinical data quality, accuracy, and uniformity throughout the study lifecycle.
• Assist in data validation, create transfer specifications, and support reporting for regulatory submissions.
• Identify and resolve data discrepancies ensuring timely delivery of study objectives.
• Perform extract, transform, and load (ETL) operations on clinical data sets.
• Generate edit checks, clinical listings, and report outputs.
• Review work performed by supporting programmers and act as the primary clinical programmer for assigned studies.
• Participate actively in study team meetings, contributing to decision-making and status updates.
• Effectively manage timelines and assigned study-related deliverables.

Required Qualifications and Skills

• Bachelor's degree in Mathematics, Computer Science, or related field.
• 2 to 8 years of experience in clinical SAS programming or database management.
• Proficiency in Clinical SAS, data management SAS, SAS macros, and clinical SAS programming techniques.
• Familiarity with pharmaceutical clinical development processes and regulatory submission requirements.
• Good understanding of statistical methods and principles relevant to clinical studies.
• Experience with clinical data validation, documentation, and data quality monitoring.
• Knowledge of FDA 21 CFR Part 11 compliance, electronic data capture (EDC) systems, and clinical data management tools.
• Preferred experience with biomarker data and clinical study designs.
• Strong verbal and written communication capabilities.

Work Location and Mode

Positions available in Kochi, Bangalore, Mumbai, and Kolkata with a hybrid working arrangement.

Eligibility

Applicants must have a Bachelor of Pharmacy (B.Pharma) degree in any specialization.