370991BR
May 31, 2024
Ireland
Summary
-Responsible for all statistical programming/data review reporting and analytics development aspects of assigned studies or project-level activities. Acts as a key contributor in ensuring that drug-development plans are executed efficiently with timely and high quality deliverables.
About the Role
Major accountabilities:
Work Experience:
- Responsible for planning, monitoring, documenting of projects and analysis of information -Co-ordinate activities of all programmers either internally or externally assigned to the study/project work -Make statistical programming/data review reporting development recommendations at study level.
- Contribute to project level standards -Review and discuss data structures and participate in data review activities.
- Provide input into statistical programming/data Reporting & Analytics solutions and/or ensure their efficient implementation -Responsible for development of programming specifications of analysis datasets or user requirement documentation -Contributes to some cost center goals and objectives -Broadens technical knowledge via departmental activities, literature reading and experiential learning.
- May train junior.
- new team members -Skilled in collaboration across project team(s) -Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)
- Achieve high level of quality, timeliness, cost efficiency and customer satisfaction across functional activities and deliverables.
- Adherence to Novartis policy and guidelines -Customer / partner feedback and satisfaction
Work Experience:
- Statistical Programming.
- R&D Portfolio Management.
- Clinical Research Phases.
- Clinical Trial Design, Data Review & Reporting.
- Innovative & Analytical Technologies.
- Regulatory Submissions.
- Biostatistics.
- Data Management & Systems.
- NA.
- English.
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Development
Innovative Medicines
Ireland
Dublin (Country President Office (CPO))
IE02 (FCRS = IE002) Novartis Ireland Ltd
Research & Development
Full time
Regular
No
