At Veeva, we build enterprise cloud technology that powers the biggest names in the pharmaceutical, biotech, consumer goods, chemical & cosmetics industries. Our customers make vaccines, life-saving medicines, and life-enhancing products that make a difference in everyday lives. Our technology has transformed these industries; enabling them to get critical products and services to market faster. Our core values, Do the Right Thing, Customer Success, Employee Success, and Speed, guide us as we make our customers more efficient and effective in everything they do.
Veeva Vault Clinical Data Management System (CDMS) is changing the way clinical data is managed in the industry. Vault CDMS combines EDC, coding, data cleaning, and reporting into one application. The days of complex integrations limiting clinical data availability are gone; now research teams can make faster and more informed decisions.
As a key member of our CDMS Professional Services team, the Senior Consultant will be responsible for four main things as part of a Clinical Study build. 1. Understanding our customers’ data management challenges and needs, establishing and maintaining project scope, timelines, financials, and facilitating communication to ensure a successful implementation based on the customers’ requirements. 2. Leading and mentoring talented project team members implementing and configuring the solution. 3. Train and mentor customers who are working with the Vault CDMS application or are new to clinical trials. 4. Becoming a customer advocate, working closely with other Veeva teams (Product, Sales, Strategy) to ensure customer success today and in the future.
Veeva’s headquarters is located in the San Francisco Bay Area with offices in more than 15 countries around the world.