The businesses of Merck KGaA, Darmstadt, Germany
Senior Data Standards Expert (all genders)
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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.
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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.
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Your Role
In your role as Senior Data Standards Expert / CRF Designer (all genders), you will:
- Shape and maintain clinical data standards
- Design high-quality electronic case report forms for global clinical studies
- Lead complex study builds in electronic data capture systems
- Manage metadata and standards libraries
- Ensure alignment with CDISC, CDASH and SDTM requirements
- Oversee standards deliverables from external partners
- Support submission readiness
- Manage study-level standards exceptions
- Apply quality-by-design principles
You will be working across clinical data management, programming, regulatory and technology teams, mentoring colleagues and driving improvements in standards governance, automation and emerging data formats.
This role requires to be on-site in our office in Feltham, UK for 3 days per week.
Who You Are
- Advanced degree in life sciences, computer science or equivalent experience
- 6 - 8 years in clinical data standards, data management or eDC design
- Strong CDISC, CDASH, SDTM, metadata and CRF design expertise
- Experience leading complex studies and cross-functional projects
- Knowledge of regulatory submissions and validation tools
- Clear communication, problem-solving and mentoring skills
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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!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
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