Experteer Overview
As a Senior Consultant, you help customers maximize Vault CDMS for CDMS-enabled trial execution. You act as a trusted advisor, aligning trial designs with client goals and providing training and mentorship. You lead database development and coordinate data transfers with providers and vendors. You contribute to process improvements and share learnings with the product team to shape best practices in clinical data management.

Compensaciones / Incentivos
• Serve as trusted advisor to customers and clinical sites; configure trial designs to meet goals and provide training
• Interpret protocol requirements and project specs, applying industry and Veeva best practices
• Lead database development per project plan; coordinate with sponsor, CRO, and other vendors
• Coordinate with clinical data providers (central labs, ECG, eCOA, IRT, etc.) to configure data transfers
• Configure forms, rules, and study items in Vault CDMS; create SQL-based listings for data cleaning
• Conduct on-site or remote UAT; manage feedback, issues, and study acceptance
• Support requirements gathering and specs writing for study integrations and go-live activities
• Flag risks and contingency plans to PM to ensure regulatory and Veeva compliance




• Contribute to process/product initiatives and support developers/testers through lifecycle
• Share data management activities and end-user feedback with Vault CDMS product team
• Configure and support data imports into Veeva DQS

Responsabilidades
• 5+ years of experience with EDC clinical software and end-to-end data management
• Solid understanding of clinical trial processes around data collection and review
• Programming experience in SAS, R, JSON, Python, or SQL; ability to learn new SQL-based languages
• Background in life sciences industry (pharma, biotech, medical device, CRO, or public health) with project lifecycle experience
• Experience in a customer-facing role within software professional services or consulting
• Ability to work independently and 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 plus local public holidays
• pension / retirement plan contributions
• 1% charitable giving program

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