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Tier-1 employer, metro location, mid-level role but niche Veeva specialization reduces applicant density.
Highly pharma- and Veeva-specific (CSV, GMP, Vault), making skills less transferable across industries.
Multiple explicit requirements: Veeva certifications, CSV experience, and domain-specific Vault experience increase filtering rigor.
Accountable for end-to-end delivery and operational management of the Veeva Clinical and Platform portfolio including implementing new features and maintaining system reliability.
Lead and mentor a team of 6+ Veeva developers and testers in a matrix setup, ensuring timely delivery of general, operational, and project releases.
Collaborate with internal teams, contractors, and Veeva product team to design and deliver technical solutions meeting business and regulatory requirements.
5+ years of experience with validated systems and Computer System Validation (CSV).
3+ years of experience with Veeva Vault Quality, Regulatory, Clinical, and Platform domains.
Requires Veeva White Belt certification; ability to obtain and maintain Veeva Associate Administrator Level certification.
Experience leading small teams in a matrix environment and managing both individual contributors and cross-functional collaboration.
Experienced in GMP, Quality, Regulatory, and Clinical Management Systems within the Veeva Vault platform, with a focus on both implementation and operational excellence.
Skilled in stakeholder communication and coordination to achieve successful delivery and adoption of Veeva technology assets.
Capable of analyzing complex operational and technical issues and delivering moderately complex solutions while driving process improvements.