Clinical Programmer

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: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

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