OverviewIn this role you ensure high-quality, compliant requirements for clinical trial systems that support a general data repository.
You bridge clinical operations and IT to improve specification governance, traceability, and data platform reliability.
You will lead workshops, identify gaps, and translate complex rules into precise, actionable documentation.
This position offers cross-functional impact in a regulated, global setting with opportunities to shape data-driven clinical trial execution.
ResponsabilidadesReview, improve, and create Functional Requirement Specifications to align business intent with technical feasibility
Identify gaps, resolve ambiguities, and simplify complex business rules
Facilitate structured requirement reviews with cross-functional stakeholders
Drive improvements to documentation standards, traceability, and requirement governance




Influence reliability and scalability of data platforms underpinning clinical trial operations
Requisitos principales5+ years as a Business Analyst in complex, cross-functional environments
3+ years of hands-on experience with clinical trial data and processes
Experience facilitating requirement workshops and stakeholder reviews
Practical experience with data platforms, system integrations, and APIs
Experience in regulated environments with Good Practice standards (validation, traceability, change control)
Degree in Information Technology, Life Sciences, Business, or related field, or equivalent
AI literacy and ability to assess AI-driven tools responsibly
facilitation and workshop leadership
strong analytical mindset
attention to detail
functional requirements specification
data platforms
system integrations

📌 Requirements Engineer (España)
🏢 Merck
📍 España