Back
Metro location and mid-level generalist title increase competition, but niche Veeva specialization limits applicants.
High due to specialized Veeva Vault, CSV, and regulated pharmaceutical domain expertise.
Multiple mandatory filters: 5–7 years, Veeva/CSV experience, and required Veeva certifications.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Lead delivery and management of Veeva Clinical and Platform projects, including implementation and operations.
Manage and mentor a matrix team of 6+ Veeva developers and testers in India center across Quality, Regulatory, Clinical, and Platform domains.
Oversee technology asset lifecycle including maintenance, security assessments, regulatory risk assessments, incident response, and timely release delivery.
5+ years of validated system Computer System Validation (CSV) experience.
3+ years of experience with Veeva Quality, Regulatory, Clinical, and Platform Vault systems.
Veeva White Belt certification required; Veeva Associate Administrator Level certification to be obtained/maintained.
Experience in GMP, Quality, Regulatory, Clinical Management Systems, and working in matrix team environments with people management responsibilities.
Experienced in leading small teams within matrix setups focused on Veeva Vault implementations and operations in healthcare or pharmaceutical industries.
Strong ability to collaborate with cross-functional teams including IT business partners and Veeva product teams to deliver and support technology solutions.
Capable of designing technical solutions, making operational decisions affecting multiple teams, and driving continuous improvement in processes and team capabilities.