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Teva Associate Manager Systems Processes PM 
United States, Pennsylvania, East Bradford Township 
847420620

14.07.2024

The Associate Manager, Systems and Processes PM is responsible of supporting the planning, development, implementation and ongoing management of business processes and other requirements of IT systems to enhance business performance and operational excellence for R&D Global Clinical Operations Innovative medicines, Biosimilars and Generics.
This includes but is not limited to: support with management of operational interfaces (internal and external), support operational new/ongoing cross study, cross functional processes and system related processes.


How you’ll spend your day
  • Participate in planning, development, implementation and ongoing management of cross study, cross functional, operational and system related projects.
  • Supporting department related tasks and projects by collaborating with all identified stakeholders- Teva internal functions: R&D IT, IT QA, DM, CM, CP, CSC, study managers, CTAs and other study and Teva functions as needed. Collaborate with Teva external suppliers: technology vendors, CROs etc.
  • Development of required training materials and support end users for usability of ongoing system related processes
  • Analyze and optimize organizational processes and workflows, business system requirements and operational processes
  • Support with ongoing interfaces set up and management
  • Data entry in TGEC (Veeva Clinical Suite) as per needed
  • Resolve data gaps in TGEC
  • Work as part of a professional team with technology
Your experience and qualifications

Education Required: Bachelor’s degree in industrial/bio medical Engineering, MIS (Management Information Systems), computer science, healthcare/bio-informatics, or equivalent combination of education and related work experience

Experience Required: 2-3 years of demonstrated experience in supporting technology systems in healthcare or pharma- must.
• Technical orientation to systems- must
• English in high level - must

Experience Preferred: Experience in project management, organization and tools - significant advantage
Specialized or Technical Knowledge Licenses, Certifications needed: Knowledge of standard Windows programs (Word, Power Point, Outlook etc.).

Functional Knowledge: Understanding of clinical drug development
Knowledge demonstrated in clinical trials processes and process improvement

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