• Lead requirements-gathering sessions to understand customers’ data management needs and challenges. Offer guidance and direction to ensure that the clinical trial is designed with the deliverable in view
• Understand our customers’ clinical trial protocol requirements, create specifications, and implement a study design with the Vault CDMS application
• Adhere to Good Clinical Data Management Practices and Veeva standards to optimize value
• Author all specification documents used by team members and configure Veeva products during the development phase of the project
• Train and mentor customers and clinical sites who are working with the Vault CDMS application or are new to clinical trials
• Support the requirements gathering and specification creation process for all study integrations
• Lead customer requirement and testing sessions
• Notify project management of project risks and develop contingency plans as necessary
• Deliver post go-live configuration changes.

• 5+ years experience in end-to-end data management-related activities in EDC (database design and configuration, data collection, data analysis, query resolution, datasets, statistical reporting)
• Experience in interpreting clinical protocols and translating requirements into software specifications, including writing and reviewing technical documentation
• Experience in designing forms and rules in EDC, as well as understanding how data is managed, cleaned, and reported
• Strong understanding of data management standards and guidelines (GCDMP, CDISC, SDTMIG, CDASH)
• Experience in a customer-facing role, preferably with a software professional services or consulting organization
• Proven track record of meeting project timelines/deliverables and attention to detail, process, deadlines, and quality results,
• Ability to travel up to 25% (may include international)

• Hands-on data management experience
• Experience working with system integrators for IVRS, medical coding, e Source, CTMS, e TMF, and other clinical technologies
• Experience with defining data standards and libraries
• Life Science, computer science, or related degree
• Saa S/Cloud experience in the delivery of clinical trials
• Experience with training for clinical sites and at investigator meetings
• Fluency in one or more of the following languages: German, French, Spanish, Italian

Work Where It’s Best for You

Work Anywhere means you can work in an office or at home on any given day. It’s about getting the work done in the way and place that works best for each person. This applies across all locations and departments.
Work Anywhere does not mean work at any time. We have predictable core hours where employees are generally available for meetings and collaboration. Employees are focused and available during core hours.
We invest in our offices to make them places where our employees like to go. If you work in the office three or more days a week, you will have a dedicated office workspace. Our offices function as hubs to draw people in, create social bonds, and where random connections and mixing of ideas happen. We’re investing more in offices, culture, and offsite meetings, not less.
Product teams are organized in regional product hubs for optimal collaboration and live within a time zone of their hub. Our current product hubs are located in Pleasanton, Columbus, Boston, Kansas City, New York City, Raleigh, and Toronto. We create opportunities for teams to get together in person regularly.
Customer-facing roles, such as Sales and Professional Services, live near and/or travel to their customers.
When an employee moves within a country it does not cause a change in salary. Where you live impacts you and your family. Not knowing if your compensation will change if you move can cause stress and uncertainty for everyone. We wanted to eliminate that.
Work at Veeva. Work where it’s best for you.