Principal Ontologist, Preclinical Sciences & Translational Safety

Johnson & Johnson

Confirmed live today High trust
Hybrid

Quick summary

Work type
Hybrid
Location
Spring House, PAMadrid, Madrid, SpainBeerse, Antwerp, BelgiumCornellà de Llobregat, Barcelona, Spain
Employment
Full-time
Posted
2 days ago
Freshness
Confirmed live today
Closes
Nov 13, 2026

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Similar $216k
$149k $278k
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About Johnson & Johnson

Johnson & Johnson is a multinational corporation operating in three main segments: consumer health products, pharmaceuticals, and medical devices, known for brands like Tylenol, Band-Aid, and Janssen. Industry: Pharmaceuticals & Medical Devices

Johnson & Johnson currently has 56 open roles on FindRole.

Listed pay typically runs $117,000–$201,250 across 43 roles with salary data.

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At a glance

TL;DR · Principal Ontologist, Preclinical Sciences & Translational Safety

The Principal Ontologist joins the R&D DDSAI team to develop and support ontologies, controlled vocabularies, and semantic data standards for Preclinical Sciences & Translational Safety. This role involves designing, testing, and maintaining ontology modules to standardize terminology across toxicology, safety assessment, pharmacokinetics, and translational research. You will translate scientific knowledge into reusable semantic models, harmonize terminology across diverse data sources, and collaborate with data engineers to incorporate these mappings into metadata systems and scientific workflows. Key technical requirements include proficiency with ontology development tools like Protégé, OWL/RDF, version control, and scripting for data transformation. You will solve complex scientific data challenges by establishing shared definitions that connect evidence across the R&D pipeline, ensuring datasets retain the necessary context for reliable interpretation, reuse, and AI-supported research.

What you'll do

  • Design, develop, test, and maintain ontology modules and controlled vocabularies for PSTS scientific workflows.
  • Translate scientific concepts and experimental contexts from subject matter experts into well-structured semantic models.
  • Harmonize terminology across projects and data sources while developing mappings to external standards.
  • Support project teams with requirements gathering, semantic annotation, data mapping, and issue resolution.
  • Partner with data engineers to incorporate ontology terms into data products and metadata systems.
  • Establish shared definitions to connect PSTS evidence with upstream discovery and downstream development data.
  • Apply modeling guidelines, version control, and change management practices to maintain traceable definitions.
  • Evaluate approaches for terminology extraction and mapping automation to support analytics and AI readiness.

What we're looking for

  • Master’s degree or Ph.D. in Biomedical Informatics, Bioinformatics, Life Sciences, Engineering, or a related discipline.
  • Hands-on experience developing and maintaining ontologies, controlled vocabularies, semantic models, or knowledge graphs for scientific or biomedical applications.
  • Experience with ontology development tools such as Protégé, OWL/RDF, version control, and scripting for data transformation and validation.
  • Ability to translate scientific requirements into clear, reusable semantic structures.
  • Strong communication, problem-solving, and stakeholder engagement skills.
  • Ability to manage multiple workstreams and deliver practical solutions in a matrixed environment.
  • Experience with pharmaceutical R&D data, particularly toxicology, safety sciences, ADME/DMPK, pathology, or translational research (preferred).
  • Familiarity with biomedical ontologies, regulatory data standards (CDISC/SEND), and FAIR data principles (preferred).

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