9 Jobs für Clinical Drug Toxicologist
Stellenangebote Clinical Drug Toxicologist Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
• Opfikon, Zürich Zuerich
[. .. ] Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description Summary : Project Toxicology Role [...]
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[...] : The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. The role is responsible for the design, adequate budgeting, and monitoring of non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment Regulatory Toxicology Role : The Principal Toxicologist will compile Toxicological Risk Assessments across multiple drug development projects supporting R D, CMC and Quality and/or will compile nonclinical submission documents across all projects. Main Responsibilities : [. .. ]
Job vor 6 Tagen bei Jobleads gefunden
• Lausanne, Waadt
Führungs-/ Leitungspositionen
[. .. ] to adapt to nuanced and nascent regulatory spaces. You will be instrumental in building value propositions and supporting earlystage product concepts with rigorous toxicological science. Youll bring [...]
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[...] deep expertise in drug development, regulatory frameworks, and preclinical study oversight, balancing safety and efficacy considerations. Your Responsibilities Prepare complex toxicological risk and hazard assessments for innovative botanical drugs and consumer products, including ADE/ PDE determination and safety risk evaluation using in vitro, in vivo, and insilico approaches. Interpret preclinical studies to assess safety [. .. ] PK, genotoxicity, reproductive and embryotoxicity) in line with regulatory standards and timelines. Drive functional area development and implement new methodologies and techniques. Collaborate with crossfunctional teams (Scientific Innovation, Product Development, Clinical) and manage thirdparty CROs for toxicity and efficacy testing. Does This Sound Like You? Academic credentials: Masters degree in life sciences (pharmacy, biochemistry, medicine, biology, veterinary) is essential; Ph D strongly preferred. Professional certifications: ERT (European Registered Toxicologist) or DABT (Diplomate of the American Board of Toxicology) strongly desirable. Industrial expertise: Proven experience in toxicological risk assessments of natural products or biopharmaceuticals, with demonstrable success in preclinical study oversight. Regulatory mastery: Deep understanding of drug development and commercialisation processes, regulatory frameworks, and study design methodology. Strategic leadership: Experience [. .. ]
Job vor 10 Tagen bei Jobleads gefunden
[. .. ] the whole value chain from target assessment to onmarket and beyond. The position is within the Translational Safety Assessment Chapter in Pharmaceutical Sciences. We drive the nonclinical [...]
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[...] safety assessment of drug candidates from small molecules to complex biological products through all the discovery and development phases at Roche. The Opportunity We are offering an outstanding opportunity for a Project Toxicologist to work with multidisciplinary teams in preclinical drug discovery and development with a focus on mechanistic, translational and regulatory aspects. Your main responsibilities The development and execution of an integrated and scientifically sound nonclinical safety strategy from target assessment through clinical trial conduct to registration Representing Pharmaceutical Sciences in Global project teams and acting as a key contributor to the selection and timely development of potential new medicines through close interactions with discovery therapeutic areas, and affiliated nonclinical, clinical development and regulatory functions Steering nonclinical safety evaluations for potential inlicensing opportunities, [. .. ]
Job am 16.11.2025 bei Jobleads gefunden
Project Toxicologist with large molecule experience
• Basel, Basel- Stadt
[. .. ] development across the whole value chain from target assessment to on-market and beyond. The position is within the Translational Safety Assessment Chapter in Pharmaceutical Sciences. We drive [...]
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[...] the non-clinical safety assessment of drug candidates from small molecules to complex biological products through all the discovery and development phases at Roche. The Opportunity We are offering an outstanding opportunity for a Project Toxicologist to work with multidisciplinary teams in preclinical drug discovery and development with a focus on mechanistic, translational and regulatory aspects. Your main responsibilities in this position are: The development and execution of an integrated and scientifically sound nonclinical safety strategy from target assessment through clinical trial conduct to registration Representing [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
[. .. ] biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description Summary Project Toxicology [...]
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[...] Role: The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. The role is responsible for the design, adequate budgeting, and monitoring of nonclinical safety studies conducted [. .. ] Development representative in Research Project teams. Design, oversee, and interpret nonclinical safety studies (GLP and non GLP) to support regulatory submissions and drug development. Develop and implement toxicology strategies aligned with clinical development plans. Proactively identify and manage safety risks and liabilities early in development across therapeutic modalities. Prepare and review regulatory nonclinical submission documents. Collaborate with internal stakeholders including pharmacology, PK, clinical, regulatory, and CMC teams. Present integrated safety assessments to senior management and at project milestone reviews. Compile toxicological risk [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
Project Toxicologist with large molecule experience
• Basel, Basel- Stadt
Project
Toxicologist with large molecule experience page is loaded # # Project Toxicologist with large molecule experiencelocations: Basel: Welwyntime type: Tempo integralposted on: Publicado hojejob requisition id: 202511-128640At Roche [...]
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[...] you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine [. .. ] development across the whole value chain from target assessment to on-market and beyond. The position is within the Translational Safety Assessment Chapter in Pharmaceutical Sciences. We drive the non-clinical safety assessment of drug candidates from small molecules to complex biological products through all the discovery and development phases at Roche. # # # The Opportunity We are offering an outstanding opportunity for a Project Toxicologist to work with multidisciplinary teams in preclinical drug discovery and development with a focus on mechanistic, translational [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Regulatory Toxicology
• Zürich
[. .. ] dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description Summary:Project Toxicology [...]
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[...] Role: The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. The role is responsible for the design, adequate budgeting, and monitoring of non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment Regulatory Toxicology Role: The Principal Toxicologist will compile Toxicological Risk Assessments across multiple drug development projects supporting R D, CMC and Quality and/or will compile nonclinical submission documents across all projects. Main Responsibilities:Serve as the [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Regulatory Toxicology
• Glattbrugg, Zürich
[. .. ] thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description [...]
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[...] Summary The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. The role serves as the primary toxicology representative on interdisciplinary project teams, leads the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. Responsibilities include design, budgeting, and monitoring of nonclinical safety studies in GLP and non GLP environments. The role [. .. ] Development representative in research project teams. Design, oversee, and interpret nonclinical safety studies (GLP and non GLP) to support regulatory submissions and drug development. Develop and implement toxicology strategies aligned with clinical development plans. Proactively identify and manage safety risks and liabilities early in development across therapeutic modalities. Prepare and review regulatory nonclinical submission documents. Collaborate with internal stakeholders including pharmacology, PK, clinical, regulatory, and CMC teams. Present integrated safety assessments to senior management and at project milestone reviews. Compile toxicological risk [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Toxicology
• Zürich
[. .. ] dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Position Description Summary:Project Toxicology [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Role: The Principal Toxicologist will lead and manage nonclinical safety strategies across multiple drug development projects. This role serves as the primary toxicology representative on interdisciplinary project teams, will lead the Nonclinical Expert Team (NCET) and provides scientific leadership from early discovery through regulatory submission and market authorization. The role is responsible for the design, adequate budgeting, and monitoring of non-clinical safety studies conducted internally and externally both in a GLP and non-GLP environment Regulatory Toxicology Role: The Principal Toxicologist will compile Toxicological Risk Assessments across multiple drug development projects supporting R D, CMC and Quality and/or will compile nonclinical submission documents across all projects. Main Responsibilities:Serve as the [. .. ]
Häufig gestellte Fragen
Wieviel verdient man als Clinical Drug Toxicologist pro Jahr?
Als Clinical Drug Toxicologist verdient man zwischen EUR 60.000,- bis EUR 100.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Clinical Drug Toxicologist Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 9 offene Stellenanzeigen für Clinical Drug Toxicologist Jobs.
In welchen Bundesländern werden die meisten Clinical Drug Toxicologist Jobs angeboten?
Die meisten Stellenanzeigen für Clinical Drug Toxicologist Jobs werden derzeit in Niedersachsen (5 Jobs), Nordrhein-Westfalen (0 Jobs) und Bayern (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Toxicologist Jobs?
Clinical Drug Toxicologist Jobs gehören zum Berufsfeld Pharmazie.
