Responsible for developing and maintaining real-time transfer of critical non-clinical study data from internal studies, contract research laboratories, and other external partners into Novartis data systems
Job Summary
Responsible for developing and maintaining real-time transfer of critical non-clinical study data from internal studies, contract research laboratories, and other external partners into Novartis data systems.
Establishes and facilitates internal data QC and source-data verification processes to ensure consistency with data and to improve data quality by minimizing incidences of incomplete or inaccurate data.
Meets stakeholder data needs by enabling data mining and visualization to address key scientific questions.
Matching Summary
Responsible for developing and maintaining real-time transfer of critical non-clinical study data from internal studies, contract research laboratories, and other external partners into Novartis data systems.
Skills & Requirements
Must-have
Preclinical data management
Data quality control processes
Business Intelligence data visualization tools
Experience with LIS systems
Handling large pharmaceutical data sets
Data mining and visualization
Nice-to-have
Scripting experience with Python or R
Effective organizational skills
Excellent interpersonal and communication skills
Strong attention to detail
Broad understanding of scientific operations
Familiarity with CDISC SEND data
Microsoft Windows-based software skills
Key Requirements
Graduate/Postgraduate in Life Sciences or Computer Science
5/3 years relevant experience in preclinical data management
Experience with clinical pathology and related pharmaceutical data
Experience using LIS, particularly Pristima or Provantis
Competence with Business Intelligence visualization tools