Manager, Industry Solutions, Veeva Life Science
- 6+ years experience with relevant consulting experience.
- 4+ years of Life Sciences industry experience in the Pharma ceutical R&D regulatory affairs function to include:
- Veeva Vault implementations of Veeva RIM, Clinical, Quality, and/or Safety
- Experience with deploying AI/GenAI capabilities for regulatory content generation, regulatory intelligence, clinical trial optimization
- digital transformations / innovations
- Understanding of Veeva data models, regulatory data structures, standards, governance and regulatory filing requirements
- submissions management, labeling, CMC change control and/or LCM processes
- submissions packages
- 1+ years experience leading, managing and delivering engagements end-to-end with resources in multiple locations
- Bachelor's Degree
- Ability to travel up to 50% on average, based on the work you do and the clients and industries/sectors you serve
- Limited immigration sponsorship may be available
- Experience leading, managing and delivering complex consulting engagements with resources in multiple locations
- Ability to orchestrate, lead, and influence virtual teams, ensuring successful implementation of customer projects
- Demonstrated experience with management and delivery of multiple strategic engagements for large global organization
- Presentation skills with a high degree of comfort with both large and small audiences
- Strong problem solving and troubleshooting skills with the ability to exercise mature judgment
- Veeva certification strongly preferred
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