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Requirements Engineer - Clinical Trial Systems

Hybrid in Mollet del Valles·Added 4 days ago (last checked 26 Oct)

Merck

33 open roles

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Our summary

Work mode: Hybrid, Mollet del Valles
Experience: 5+ years
Education: University degree

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Skills

Requirements

What we're looking for

You bring 5 or more years of experience as a Business Analyst, with a strong track record of delivering high-quality requirement specifications in complex, cross-functional environments. A professional certification such as Certified Business Analysis Professional, PMI Professional in Business Analysis, or International Requirements Engineering Board certification is an advantage.
You have 3 or more years of hands-on experience with clinical trial data and processes, giving you a solid understanding of how data flows through clinical operations and what is required to support compliant, audit-ready systems.
You are skilled at facilitating requirement workshops and stakeholder reviews, translating diverse perspectives into clear, consistent, and actionable documentation.
You have practical experience working with data platforms, system integrations, and application programming interfaces, and you understand the technical constraints that shape feasible requirements.
You have worked in regulated environments and are familiar with Good Practice standards applicable to clinical data systems, including the expectations around validation, traceability, and change control.
You bring strong analytical skills and a meticulous attention to detail, with the ability to identify inconsistencies, redundancies, and gaps across large sets of requirements.
You hold a degree in Information Technology, Life Sciences, Business, or a related field, or bring equivalent professional experience that demonstrates the same depth of knowledge.
You demonstrate AI literacy: you understand how artificial intelligence technologies work, their practical applications and limitations, and the ethical considerations around bias, fairness, privacy, and accountability - enabling you to critically assess AI-driven tools and make informed, responsible decisions in your role.

The role

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your Role: at the heart of clinical data management lies a critical challenge: turning complex, evolving business needs into precise, actionable system requirements. As a Requirements Engineer for Clinical Trial Systems, you will play a pivotal role in shaping the quality and integrity of a global Operational Data Repository programme - directly enabling faster, more reliable clinical trial execution across the organisation.

What you'll do

In this role, you will own the review, improvement, and creation of Functional Requirement Specifications, ensuring they are precise, complete, and aligned with both business intent and technical feasibility. You will identify gaps, resolve ambiguities, and simplify complex business rules without losing their essential meaning. Working at the intersection of clinical operations and information technology, you will facilitate structured requirement reviews with cross-functional stakeholders and drive meaningful improvements to documentation standards, traceability, and requirement governance. Your work will directly influence the reliability and scalability of the data platforms that underpin clinical trial operations.

Hiring process

2 steps2 interviews

Online application
Application review
Behaviour-based interviews
With HR team and hiring managers
Consistent behaviour-based questions about your experience, skills and attitude; by phone, video and/or face to face.
Assessment centre
Not every role
Half-day event assessed against behavioural criteria; may include presentations, group exercises, case studies and role plays.

Expect to hear back within about two weeks of submitting an application.
Dress code and interview details are confirmed by the recruiter with the invitation.

Hiring process

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

About Merck

Merck is a global science and technology company headquartered in Darmstadt, Germany, operating across healthcare, life science, and electronics. With over 60,000 employees worldwide, it is one of the world's largest pharmaceutical and chemical companies, known for innovative medicines, laboratory solutions, and advanced materials. The company's life science division provides products and services for research and bioproduction, while its healthcare segment focuses on oncology, immunology, and neurology.

In Spain, Merck has a significant presence with offices in Madrid and Barcelona, supporting its healthcare and life science operations. The company is known for a collaborative and international work culture, offering opportunities for professionals in areas like data science, AI, software engineering, and healthcare quality. For international hires, Merck provides a dynamic environment with a strong emphasis on innovation and professional development, making it an attractive employer for those looking to advance their careers in Spain.

Industry: Life Science
Founded: 1668
Employees: 50,000–100,000
Headquarters: Darmstadt, Germany
In Spain: Madrid, Barcelona

Good to know if you are moving

Merck is a global leader in life science and healthcare, offering international career opportunities.
The company has a strong presence in Spain, with offices in Madrid and Barcelona, providing a base for professionals in the region.
Merck emphasizes innovation and research, with many roles in AI, data science, and engineering.
The company offers internships and trainee programs, ideal for early-career professionals.
Merck's work culture is collaborative and international, with English often used in professional settings.

In their own words

About the company & team

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

All open roles at Merck