REQ-10006081
May 31, 2024
United Kingdom
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.
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Development
Innovative Medicines
United Kingdom
Home Worker
GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.
Research & Development
Full time
Regular
No