Overview

In this role you ensure high-quality, compliant requirements for clinical trial systems that support a global 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, integral setting with opportunities to shape data-driven clinical trial execution.

Responsabilidades

- Review, 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 principales

- 5+ 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 - Clinical Trial Systems - Merck (Mollet del Vallès)
🏢 Merck
📍 Mollet del Vallès