Data and Analytics Systems and Processes, Netanya (February 2025)

Responsibilities:

  • Management and implementation of reporting and analytics mechanisms and tools including requirements, definition, configuration, testing and validation
  • Initiate activities related to data integrity and capture. Ensure data received and captured in global clinical operation systems is accurate and complete
  • Support for GCO Metrics, vendor metrics, oversight methodologies and identify and use industry benchmarks to evaluate process success and business performance in different fields
  • Development and implementation of organizational surveys to ensure consistency and appropriate levels of performance oversight
  • Support systems and processes team in the development of systems including analysis, design, development, implementation and support of business processes and information solutions (new and ongoing)
  • Support initiation and implementation of AI/ML and BI capabilities within GCO
  • Collaborate with Teva internal interfaces (IT, clinical operation, clinical development etc) and external suppliers (CROs, Suppliers etc.) for supporting department related tasks and projects
  • Develop departmental Job Aids and WI, as needed.
  • Work as part of a professional team with technology
  • Other tasks assigned by direct manager or as business needs require.

Requirements:

  • A Bachelor’s or higher degree in industrial/biomedical Engineering, MIS (Management Information Systems), computer science, healthcare/bio-informatics,
  • or equivalent combination of education and related work experience
  • up to 3 years’ experience working in data driven environment as data analyst/project manager/data engineering, or similar in pharmaceutical industry
  • Proficiency with programming languages
  • Ability to effectively interact with and influence others without direct reporting relationships.
  • Good verbal and written communication skills in English
  • Experience developing AI/ML projects
  • Experience working in a global company/environment
  • Knowledge of advanced Microsoft programs- PowerApps, PowerBI, Co-pilot etc
  • Programming capabilities – Excel VBA, SAS, SQL- advantage
  • Experience working with “Veeva” platforms- advantage
  • Understanding of clinical drug development
  • Knowledge demonstrated in clinical trials processes and process improvement- advantage

Send CV and job title to: [email protected]