Veeva Quality Assurance Specialist

6 days ago


Philadelphia, Pennsylvania, United States University of Pennsylvania Full time
Job Summary

The University of Pennsylvania seeks a highly skilled Veeva Quality Assurance Specialist to join the Abramson Cancer Center Clinical Research Unit. As a key member of the Regulatory Affairs Office, this individual will be responsible for reviewing and migrating Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.

Key Responsibilities
  • Review and itemize regulatory documentation from the current document management system
  • Migrate documents to the SiteVault platform, including person, organization, product, and study profiles
  • Assign metadata for new data fields and map existing data to unique Veeva data fields
  • Collaborate with the Veeva Quality Assurance Lead to ensure seamless implementation
Requirements
  • Bachelor's degree in a life science or human subject protection field
  • 3-5 years of research experience, with at least 2 years of regulatory experience
  • Excellent communication and writing skills, with ability to multitask and work in a fast-paced environment
  • Intermediate to expert level of function in Microsoft Office applications and team interconnectivity tools
Why Join Us?

The University of Pennsylvania offers a competitive benefits package, including excellent healthcare and tuition benefits, generous retirement plans, and a wide range of professional development opportunities. As a member of the Penn community, you'll have access to a vibrant cultural and recreational scene, with opportunities to engage with world-renowned faculty and staff.



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