Sr Python Programmer (ClinicalPharmaHealthcare)

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 midsenior individual contributor responsible for independently delivering clinical data programming transformation and review solutions in support of global clinical trials.

This role requires handson 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 ICHGCP 21 CFR Part 11 and internal SOPs
• Follow validated programming and documentation practices
• Contribute to inspectionready deliverables

CrossFunctional Collaboration

• Work closely with:
  • Data Managers
  • Clinical Programmers
  • Statisticians
  • Medical Reviewers

• Participate in crossfunctional discussions related to data issues timelines and deliverables
• Provide technical input during study startup conduct and closeout 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 handson 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

• Bachelors or Masters 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 problemsolving skills
• High attention to detail and data quality
• Effective communication with crossfunctional 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

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.