Roche développe des médicaments et des solutions de diagnostic. En Suisse, ses activités comprennent la recherche et le développement ainsi que les métiers pharmaceutiques et diagnostiques, notamment à Bâle, Kaiseraugst et Rotkreuz.
Hematology and Safety Biomarker Expert
Am I a fit — voir ma compatibilitéRoche recherche un expert en hématologie et biomarqueurs de sécurité au sein de son organisation Pharmaceutical Research and Early Development. Le poste porte sur le développement, la validation et la mise en œuvre d’essais de sécurité translationnelle, avec environ 50 % du temps consacré au travail en laboratoire. Une expertise en essais de biomarqueurs, en données de pathologie clinique et sur des plateformes numériques est requise.
Repères sur Roche Suisse
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Détails de l’offre
La description complète publiée par Roche Suisse.
Chez Roche, vous pouvez être vous-même et être apprécié pour les qualités uniques que vous apportez. Notre culture encourage l'expression personnelle, le dialogue ouvert et les connexions authentiques, où vous êtes valorisé, accepté et respecté pour ce que vous êtes, vous permettant de prospérer tant personnellement que professionnellement. Voici comment nous visons à prévenir, arrêter et guérir les maladies et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir. Rejoignez Roche, où chaque voix compte.
La position In Roche’s Pharmaceutical Research and Early Development organisation (pRED), we make transformative medicines for patients to tackle some of the world’s toughest unmet healthcare needs. At pRED, we are united by our mission to transform science into medicines. Together, we create a culture defined by curiosity, responsibility, and humility, where our talented people are empowered and inspired to bring forward extraordinary, life-changing innovation at speed.
At the intersection of science and innovation, pRED’s Pharmaceutical Sciences (PS) organisation enables the discovery and development of safe and effective therapeutics at optimal doses in relevant populations with a vision to power translation, continuously improve the accuracy of our predictions and accelerate the development of tomorrow's medicines. By seamlessly integrating our three core pillars—Translational Safety, Translational Pharmacology, and Biomarkers—we drive end-to-end asset development across the entire value chain, from target assessment to on-market support.
Our mission is to continuously improve predictive accuracy, optimise dosing strategies for the right patient populations, and accelerate the development of tomorrow's safe and effective therapeutics. This position is located in Pathology and Applied Safety Science, a department within the Pharmaceutical Sciences function. We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products during the discovery and development phases at Roche.
The Opportunity As an engaged Pathology and Applied Safety Science Hematology & Safety Biomarker Expert, you will play a pivotal role in the development, validation, and implementation of assays for translational safety assessment.
Your primary responsibility will be to propose, conduct and report relevant assays to understand mechanisms of toxicity, leveraging modern tools to maximise scientific insights, drive innovation, and advance our therapeutic pipeline in a highly collaborative environment. - Strategic Biomarker Integration & Translational Safety: Collaborate with experts to develop and execute integrated in vitro and in vivo hematology and safety biomarker strategies, provide subject matter expertise for clinical candidate selection, and deliver comprehensive safety risk assessments for regulatory documentation
(e.g., IND/CTA). - Multi-Disciplinary Laboratory Expertise: Allocate approximately 50% of working time to wet-lab work, focusing on the development and implementation of tailored in vitro and ex vivo hematology and fluid-based safety biomarker assays, as well as generating and compiling clinical pathology data (hematology, coagulation, clinical chemistry, urinalysis) for the responsible pathologist. - Digitisation, Image Analysis, and Automation: Partner with Digital Pathology and modelling experts to develop screening assays, utilise digital and data curation platforms (e.g., LIMS, SLIMS,
Arvados) to ensure streamlined data transfer and harmonised datasets, and optimise workflow integration to maximise operational efficiency. - Vendor Management, Quality, & Compliance Outsourcing & CRO Coordination: Manage external partnerships and drive the outsourcing of relevant assays to contract research laboratories (CROs), ensuring strict adherence to timelines and data quality standards. - Safety Standards: Maintain strict compliance with Safety, Health, and Environmental (SHE) regulations, actively fostering a culture of safe and responsible laboratory practices. - Interpersonal skills
& Stakeholders & Mentorship: Demonstrate highly collaborative skills across agile, cross-functional project teams within Pharmaceutical Sciences and related institutes, while supervising and training technical staff, apprentices, postdocs, or students. - Process Optimisation & External Visibility: Continuously optimise laboratory processes to improve quality, efficiency, and sample-handover timelines, while establishing robust networks with Key Opinion Leaders (KOLs) and participating in cross-industry working groups (e.g., FNIH Biomarkers Consortium, PSTC) to track scientific and regulatory trends.
Who you are - You hold a DVM (with a PhD or relevant specialisation), a PhD in Hematology, Biology, Immunology, Toxicology, or a Master’s degree combined with significant practical experience in in vivo toxicology. - You bring demonstrated hands-on experience in wet-lab environments, specifically with in vitro and ex vivo safety biomarker assays or clinical pathology data generation (such as hematology, coagulation, clinical chemistry, or urinalysis). - You possess familiarity with digital data platforms, data curation tools, or automated workflow integrations. - You have strong communication
and relationship-building skills, with an outstanding ability to collaborate effectively across multidisciplinary, global teams. - You demonstrate a continuous improvement mindset dedicated to optimising laboratory processes and mentoring emerging scientific talent.
At Roche, we aim high to deliver life-changing healthcare solutions. If you’re ready to make a meaningful impact on patients and healthcare systems worldwide, this is the place for you. Qui nous sommes Un avenir plus sain nous pousse à innover. Ensemble, plus de 100 000 employés à travers le monde sont dédiés à faire progresser la science et à garantir à chacun l'accès aux soins de santé aujourd'hui et pour les générations à venir.
Nos efforts aboutissent à plus de 26 millions de personnes traitées avec nos médicaments et plus de 30 milliards de tests réalisés avec nos produits de Diagnostique. Nous nous encourageons mutuellement à explorer de nouvelles possibilités, à favoriser la créativité et à conserver nos grandes ambitions, afin de fournir des solutions de santé qui changent des vies et ont un impact mondial. Construisons ensemble un avenir plus sain. Roche est un employeur offrant l'équité en matière d'emploi.
Prérequis
- DVM avec un PhD ou une spécialisation pertinente
- PhD en hématologie, biologie, immunologie ou toxicologie
- Master’s degree combiné à une expérience pratique significative en toxicologie in vivo
- Expérience pratique en laboratoire humide
- Expérience en essais de biomarqueurs de sécurité in vitro et ex vivo
- Expérience en génération de données de pathologie clinique
- Familiarité avec les plateformes de données numériques et les outils de curation des données
- Compétences en communication et en collaboration multidisciplinaire