Clinical Programmer

Summary

• Responsible to support all statistical programming/data review reporting and analytics development aspects of assigned studies or project-level activities.
  

About The Role

Major accountabilities:

• Uses professional concepts and company's policies and procedures to solve a variety of problems.
• Contribute to statistical programming/data review reporting and analytics development activities for clinical studies.
• Build and maintain effective working relationship with cross -functional team.
• Contribute to audit readiness of all assigned statistical programming deliverables -Comply with company, department and industry standards and processes; -Attend functional meetings and trainings -Demonstrates potential for technical proficiency, scientific creativity, collaboration with others and independent thought.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)
  

Key Performance Indicators

• Achieve high level of quality, timeliness, cost efficiency and customer satisfaction across functional Statistical Programming activities and deliverables.
• Adherence to Novartis policy and guidelines -Customer / partner feedback and satisfaction
  

Minimum Requirements

Work Experience:

• Clinical Research Phases.
• Biostatistics.
• Clinical Trial Design, Data Review & Reporting.
• Statistical Programming.
• Data Management & Systems.
• Regulatory Submissions.
• Innovative & Analytical Technologies.
• R&D Portfolio Management.
  

Skills

• Clinical Trials.
• Computer Programming.
• Data Analysis.
• Programming Languages.
  

Languages

• English.
  

Why Novartis:

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Benefits and Rewards: