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]