Principal Scientist Clinical Genomics (all genders)

TN Germany; Darmstadt; Vor Ort; EUR 80.000 - 120.000; Vollzeit

Zusammenfassung

A leading company in Clinical Genomics is seeking a Principal Scientist to lead clinical biomarker projects. The role involves collaboration with a global team to advance clinical biomarkers and technologies, ensuring quality and compliance in clinical trials.

Qualifikationen

• 5-10+ years experience in clinical/CDx/translational biomarker development.
• Hands-on expertise in assay development, validation, implementation.

Aufgaben

• Lead clinical biomarker assay strategy definition and validation.
• Manage clinical biomarker projects within quality, timeline, and budget.

Kenntnisse

Interpersonal Skills

Communication Skills

Scientific Excellence

Curiosity

Ausbildung

PhD

MD

Jobbeschreibung

Principal Scientist Clinical Genomics (all genders), Darmstadt

We have an exciting opportunity for a Scientific Associate Director to join our growing Clinical Genomics team! In this role, you will collaborate with a global team of experts to advance the 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.

You will be the technical lead for clinical biomarker assay strategy definition, development, outsourcing, and validation under CLIA/CAP and GCLP. Additionally, you will contribute to setting up clinical trial documents and manage clinical biomarker projects within quality, timeline, and budget expectations. This permanent role is based in Darmstadt, Germany, but can operate from other European locations.

Who you are:

• PhD/MD or equivalent degree
• Specialist in clinical genomics with 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