Associate Director, Veeva Study Training System Owner, Global Clinical Solutions

Tryzenoya

Warsaw, Poland
3d onsite
Clinical system lifecycle management
Veeva study training implementation
Regulated environment validation
Global Clinical Solutions drives the delivery of technology and associated processes for the R&D organisation, owning and providing industry leading technology and services on behalf of Development Operations and its internal and external Partnerships

Job Summary

  • Global Clinical Solutions drives the delivery of technology and associated processes for the R&D organisation, owning and providing industry leading technology and services on behalf of Development Operations and its internal and external Partnerships.
  • The System Owner is accountable for the leadership, lifecycle management, and continuous improvement of clinical systems, ensuring compliance with ICH/GxP requirements and alignment with industry standards.
  • The role involves close collaboration with vendors, R&D IT, functional process owners, and stakeholders to ensure customer needs are met and to enable optimal end-to-end delivery of clinical studies.

Matching Summary

Global Clinical Solutions drives the delivery of technology and associated processes for the R&D organisation, owning and providing industry leading technology and services on behalf of Development Operations and its internal and external Partnerships.

Skills & Requirements

Must-have

  • Clinical system lifecycle management
  • Veeva Study Training implementation
  • Regulated environment validation
  • Stakeholder communication and engagement
  • Project management skills
  • Continuous improvement methodologies
  • Customer service and support

Nice-to-have

  • Lean Six Sigma process improvement
  • AGILE certification (e.g. SAFe)
  • Quality management experience
  • Vendor collaboration
  • Incident and change management (ITIL)
  • Business process development
  • Strong interpersonal skills

Key Requirements

  • Bachelor of Science or equivalent experience
  • Extensive drug development experience
  • Experience in computerized system validation
  • Knowledge of GxP and regulatory requirements
  • Project management certification preferred
  • Experience with Veeva systems preferred
  • Recognised AGILE certification desirable

Work Rights

Not specified

Tailored Resume

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