Experteer Overview
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In this role, you accelerate clinical trial data management by configuring Vault CDMS and enabling EDC solutions for life sciences customers. You act as a trusted advisor, shaping study designs, supporting data transfers, and guiding teams through implementation and go-live. You will work cross-functionally with sponsors, CROs, and vendors to ensure compliant, efficient data management and delivery of value. This is a remote-friendly, customer-facing position with a focus on impact and rapid execution.
Compensaciones / Ventajas
• Act as trusted advisor to customers and sites, aligning trial designs with goals and providing training
• Interpret protocol requirements and project specs, applying industry and Veeva best practices
• Lead database development activities per project plan, coordinating with sponsor, CRO, and vendors
• Coordinate data transfers with central labs, ECG, eCOA, IRT, and other providers
• Configure forms, rules, and study items in Vault CDMS; build SQL-based listings for data cleaning
• Lead user acceptance testing (on-site or remote) and manage feedback and issue resolution




• Support requirements gathering and spec writing for study integrations and go-live
• Flag risks and design contingency plans to keep projects compliant with regulatory and Veeva procedures
• Contribute to process/product initiatives and support developers/testers throughout the lifecycle
• Share data management activities and end-user feedback with the Vault CDMS product team
• Configure and support data imports into Veeva DQS
Responsabilidades
• 5+ years of experience with end-to-end EDC clinical software
• Solid understanding of clinical trial processes around data collection and review
• Programming experience in SAS, R, JSON, Python, or SQL; ability to learn new xqbhyrx SQL-based languages
• Life sciences background with pharma/biotech/CRO or academic/public health exposure
• Experience in a customer-facing role within software professional services or consulting
• Ability to work independently and collaboratively in a fast-paced environment while meeting timelines
• Strong verbal/written communication, interpersonal, and presentation skills
• Willingness to travel up to 10% (potentially international)
Requisitos principales
• Private health insurance
• Flexible paid time off
• Pension / retirement plan contributions
• 1% charitable giving program

📌 Senior Consultant - Clinical Data Programming (Barcelona)
🏢 Veeva Systems
📍 Barcelona