Senior Consultant

Summary

Join Veeva Systems, a leading life sciences industry cloud company, as a Senior Consultant on our CDMS Professional Services team. You will be a trusted advisor to clients, ensuring their clinical trial designs leverage the full capabilities of Veeva's CDMS application. This Work Anywhere position allows flexibility to work remotely within the EU or in one of our EU offices. You will lead requirements gathering, design studies using Vault CDMS, adhere to industry best practices, and train customers. The role requires extensive experience in data management and clinical trials, along with strong communication and project management skills. Veeva offers a supportive and inclusive work environment.

Requirements

• 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)

Responsibilities

• 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

Preferred Qualifications

• Hands-on data management experience
• Experience working with system integrators for IVRS, medical coding, eSource, CTMS, eTMF, and other clinical technologies
• Experience with defining data standards and libraries
• Life Science, computer science, or related degree
• SaaS/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

Benefits

Work Anywhere company, supporting flexibility to work from home or in the office