Veeva is a mission-driven organization that aspires to help our customers in Life Sciences and Regulated industries bring their products to market, faster.
We are shaped by our values: Do the Right Thing, Customer Success, Employee Success, and Speed.
Our teams develop transformative cloud software, services, consulting, and data to make our customers more efficient and effective in everything they do.
Veeva is a work anywhere company.
You can work at home, at a customer site, or in an office on any given day.
As a Public Benefit Corporation, you will also work for a company focused on making a positive impact on its customers, employees, and communities.
The Role Do you love solving business problems with technology?
Are you an innovator?
Do you love to learn and thrive navigating new situations and environments?
Come help us transform how regulatory information is managed in Life Sciences!
Veeva's Vault RIM suite is the industry's only unified software solution that provides fully integrated regulatory information management (RIM) capabilities including data and document management, submission publishing and archival on a single cloud-based platform.
Veeva Systems is looking for Life Sciences Consultants with system implementation experience and a passion for helping customers optimize their regulatory data and document management process.
As a key member of our Professional Services team, the Consultant will be responsible for understanding our customers' Document Management (Documentum, OpenText, SharePoint), Registration Data Tracking Systems, XEVMPD, IDMP, SPL, eCTD, Submission Publishing and/or Archiving / Viewing systems.
Proven ability to collaborate with diverse stakeholders and ensure delivery to a high degree of satisfaction.
Excellent communication skills - written, verbal and formal presentation.
Technical abilities and willingness to roll up your sleeves.
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