Senior Consultant – Clinical Data Programming

About the role

Veeva Systems is seeking a Senior Consultant to help customers maximize the use of its Vault Clinical Data Management System (CDMS). The role involves configuring trial designs, providing training, and ensuring data quality for life‑science clinical studies. This is a full‑time, permanent, customer‑facing position based in Barcelona with remote work flexibility across the EU.

Key responsibilities

• Act as a trusted advisor to customers and clinical sites, configuring trial designs and providing training and mentorship.
• Interpret clinical protocol requirements, lead database development, and coordinate with sponsors, CROs, and vendors.
• Configure forms, rules, and study items in Vault CDMS and build custom SQL‑based listings for data cleaning.
• Run user acceptance testing, manage feedback, and support study acceptance.
• Configure and support data imports into Veeva DQS and flag risks to project management.

Required profile

• 5+ years of experience with EDC clinical software covering end‑to‑end data management.
• Solid understanding of clinical trial processes and data collection/review.
• Programming experience in SAS, R, JSON, Python, or SQL.
• Background in pharma, biotech, medical device, CRO, or academic/public health.
• Customer‑facing experience in software professional services or consulting.
• Willingness to travel up to 10%, including international travel.

Required skills

• SAS
• R
• JSON
• Python
• SQL
• REST APIs

What we offer

• Private health insurance
• Flexible paid time off plus local public holidays
• Pension/retirement plan contributions
• 1% charitable giving program