Principal Scientist Clinical Genomics (all genders) 1

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: We have an exciting opportunity for a Principal Scientist / Associated Director to join our growing Clinical Genomics team. In this role, you will collaborate with a global team of experts to advance implementation of clinical biomarkers and promising technologies. Our team serves as a center of excellence for clinical biomarker measurements at Healthcare R&D, dedicated to improving drug development and patient lives through smart biomarker testing solutions and new technology implementation. We work cross-functionally with research, medical, data science, regulatory, biomarker strategy and CDx experts across our clinical development portfolio. In your role you’ll be the technical lead for clinical biomarker assay strategy definition, development, outsourcing and validation under CLIA/CAP and GCLP. Furthermore, you’ll contribute to set up of clinical trial related documents and you’ll mange clinical biomarker projects within quality, timeline, and budget expectations. This permanent role is based in Darmstadt, Germany but can operate from other European or Israeli locations.

Who you are:

PhD/MD or equivalent degree
Specialist in clinical genomics with excellent hands-on expertise in assay development, validation, implementation, and data QC/interpretation
5-10+ years experience in clinical/CDx/translational biomarker development in pharma or equivalent
Excellent knowledge of current clinical genomics technology and vendor landscape
Understanding of basic regulatory requirements for assays
Good understanding of operational requirements for clinical biomarker implementation
Scientific background in oncology and/or immunology, expertise in epigenetics is a plus
Excellent interpersonal and communication skills, strong team player
Driven by scientific excellence and curiosity
Strong publication record demonstrating subject matter expertise

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it 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 our diverse team!