Data Management Consultant
6 days ago
Veeva Systems, Inc. is a pioneering force in industry cloud, driving life sciences companies to accelerate therapy delivery. With a strong commitment to Customer Success, Employee Success, and Speed, we strive for excellence.
As a Work Anywhere company, we empower your flexibility to work from home or the office, ensuring you thrive in your ideal environment.
We invite you to join us in revolutionizing the life sciences industry, dedicated to making a positive impact on our customers, employees, and communities.
The Role
Vault Clinical Data Management System (CDMS) by Veeva is transforming clinical data management. Our comprehensive solution combines Electronic Data Capture (EDC), coding, data cleaning, and reporting into one application, eliminating complex integrations that limit clinical data availability.
As a Senior Consultant with our CDMS Professional Services team, you will be at the forefront of our mission to transform the life sciences industry. You will serve as the customer's trusted advisor, ensuring their study trial design meets their goals and leverages the full benefits of Veeva's CDMS application.
This is a Work Anywhere position, allowing you to choose between remote work in the EU or working in one of our EU offices.
Key Responsibilities
- Lead requirements-gathering sessions to understand customers' data management needs and challenges.
- Adhere to Good Clinical Data Management Practices and Veeva standards to optimize value.
- Author specification documents used by team members and configure Veeva products during the project development phase.
- 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.
Requirements
- A minimum of 5 years of 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.
- A 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).
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