Sr Python Programmer (Clinical/Pharma/Healthcare)

Project Role: Software Devl Analyst 2 (Python & R Programmer) Work Experience: 5 to 8 Years Work location: Bengaluru. Work Mode: Hybrid Must Have Skills: Python is mandatory skill along with Clinical Data Management or Clinical Domain

Job Description Role Summary The Software Devl Analyst 2 (Python & R programmer) is a mid‑senior individual contributor responsible for independently delivering clinical data programming, transformation, and review solutions in support of global clinical trials. This role requires hands‑on expertise in Python and R, strong understanding of clinical data standards, and the ability to work with minimal supervision while collaborating closely with Data Managers, Clinical Programmers, Statisticians, and Medical Reviewers throughout the study lifecycle.

Key Responsibilities Clinical Data Programming & Delivery Independently develop and maintain Python and R programs for: Clinical data cleaning Data transformation Data review and analysis

Support downstream clinical data programming activities as defined in the Data Management Plan (DMP) Create and maintain data review listings, metrics, and utilities to support ongoing study conduct and database lock activities Data Review & Quality Oversight Perform detailed clinical data quality checks, trend analysis, and issue identification Support ongoing data review, reconciliation, and query resolution Ensure programming outputs meet accuracy, traceability, and audit readiness requirements Actively support interim and final database lock deliverables

Standards, Compliance & Best Practices Apply and interpret CDISC standards (SDTM) in programming and data review Ensure compliance with ICH‑GCP, 21 CFR Part 11, and internal SOPs Follow validated programming and documentation practices Contribute to inspection‑ready deliverables

Cross‑Functional Collaboration Work closely with: Data Managers Clinical Programmers Statisticians Medical Reviewers

Participate in cross‑functional discussions related to data issues, timelines, and deliverables Provide technical input during study start‑up, conduct, and close‑out phases

Automation & Continuous Improvement Develop reusable Python/R utilities and scripts to improve efficiency Contribute to process automation, standardization, and innovation initiatives Identify opportunities to reduce manual effort in data review and reporting

Required Skills & Qualifications Technical Skills (Mandatory) Strong hands‑on experience in Python and R Proficiency with: Python: Pandas, NumPy R for statistical analysis and data exploration

Strong SQL skills Proven experience working with clinical trial data Solid understanding of CDISC / SDTM standards Experience in regulated clinical data environments Tools & Systems Clinical data systems (EDC / CDB / CDMS) Data review and reporting tools Version control systems (e.g., Git) Experience supporting data ingestion and transformation workflows

Education Bachelor’s or Master’s degree in: Computer Science Statistics Data Science Life Sciences Engineering (or equivalent practical experience)

Nice to Have (Grade 140 Expectations) Ability to read and interpret SAS programs Exposure to Veeva, Oracle, Rave, or similar EDC platforms Experience with ETL processes Dashboarding / visualization exposure (Power BI, Tableau) Prior experience supporting global or complex clinical studies

Behavioural & Professional Competencies Works independently with minimal supervision Strong analytical and problem‑solving skills High attention to detail and data quality Effective communication with cross‑functional stakeholders Demonstrates ownership, accountability, and delivery focus Adaptable to changing study and project needs

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.