39 Jobs für Pharmacology Expert
Stellenangebote Pharmacology Expert Jobs
Neu Job vor 4 Std. bei Jobleads gefunden
[. .. ] creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam DAngelo, Larry Summers, and Jack [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Dorsey. Position Translational Pharmacology Expert Type Contract Compensation 175250/ hour Role Responsibilities Develop golden FIH dose rationales and escalation strategies for representative programs. Encode decision heuristics and trade-offs used by senior translational leaders into structured guidance and rubrics. Surface unwritten decision rules to understand when and why experienced teams override model-based recommendations. Create [. .. ]
Job gestern bei Mindmatch.ai gefunden
Roche
Clinical Evaluation Manager-Freelancer (m/f/d)
• AT- 9 Wien
Freiberuflich
[. .. ] activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatory-compliant Clinical Evaluation Reports (CERs) to demonstrate device safety and performance. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to post-market. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practices. Essential skills for your mission: Experience: 13 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills; Excellent written and verbal communication skills in English; Detailoriented with the ability to manage multiple tasks and deadlines; Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics; Proficiency in [. .. ]
Job gestern bei Mindmatch.ai gefunden
F. Hoffmann- La Roche Gruppe
• AT- 9 Wien
Freiberuflich
[. .. ] evaluation activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatorycompliant Clinical Evaluation Reports (CERs) to demonstrate device safety and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] performance. You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to postmarket. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practises. Essential skills for your mission: Experience: 1-3 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills Excellent written and verbal communication skills in English Detailoriented with the ability to manage multiple tasks and deadlines Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics Proficiency in [. .. ]
Job gestern bei Mindmatch.ai gefunden
F. Hoffmann- La Roche AG
Clinical Evaluation Manager-Freelancer (m/f/d)
• AT- 9 Wien
Freiberuflich
[. .. ] activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatory-compliant Clinical Evaluation Reports (CERs) to demonstrate device safety and performance. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to post-market. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practises. Essential skills for your mission: Experience: + 1-3 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: + Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: + Strong analytical and problem-solving skills + Excellent written and verbal communication skills in English + Detail-oriented with the ability to manage multiple tasks and deadlines + Capability to make risk-based decisions Technical Proficiency: + Basic [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Zug
[. .. ] symposia and publication planning. Provide input to the Medical Affairs Manager and Medical Director to develop appropriate strategic and tactical plans (e. g. MAC) for the country. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Be the team expert on all aspects of the MSL role including: process improvements and sharing of best practice. Foster a collaborative working relationship with Medical Representatives and Commercial colleagues to ensure strategies and business plans are both patient and business focused. Work with the Swiss team to bring the voice of the fieldbased [. .. ] are reported to Medical Information as per the Alnylam Adverse Event Reporting Policy. Qualifications Advanced academic background in a scientific or healthcarerelated field. A university degree in medicine, natural sciences, pharmacology, or biomedical sciences is required; an advanced degree (e. g. , Ph D or MD) is strongly preferred. Minimum of 2 years of experience in the healthcare industry or in a related role preferred; open to candidates with transferable skills. Ability to organize and prioritize own work schedule. Well developed social [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Assistant/ Associate Professor in Pharmacology/ Toxicology
• Ralingen, Rheinland- Pfalz
[. .. ] university with a distinctly multilingual and interdisciplinary character. The Faculty of Science, Technology and Medicine of the University of Luxembourg is looking for Assistant Professor (Tenuretrack) or [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Associate Professor in Pharmacology/ Toxicology or Computational Pharmacology for its Department of Life Sciences and Medicine (DLSM) . The rank will depend on the professional qualification of the candidate and in case of an appointment as Assistant Professor, an evaluation will take place after five years (Tenure track) . The Department of Life Sciences [. .. ] sciences. This strategic development requires additional expertise in teaching pharmacology in various fields (Medicine, Life sciences, Nursing, and Allied Health Professions) . About the role. . . You are an expert in Pharmacology/ Toxicology and will lead your own research group. Candidates applying computational tools (e. g. machine learning, artificial intelligence or other approaches) are also encouraged to apply. You will teach pharmacologyrelated courses in the Bachelors of Life Sciences, Medicine, Nursing, and Allied Health Professions, as well as in related [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] their consulting career path by recognizing and seeking opportunities that match their ambition and personal interests. Responsibilities Support projects for Certaras clients by working in teams with [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] other Associates, senior expert modelers, and drug development consultants. Hands-on pharmacometric modeling on client projects as a billable consultant. Conduct quality control activities on model codes and reports. May lead/coordinate company initiatives (e. g. IT, methodology, efficiency, automation, quality) . May act as the primary point of contact for clients and collaborate with a senior consultant to grow business to match their interests. Qualifications Ph D, MD, Pharm D in Bioengineering, Pharmaceutical Sciences, Pharmacology, Statistics, Applied Mathematics, Engineering, Medicine, or related field. 1 to 5 years of industry/ consulting experience working in R D, pre-clinical and clinical environments (may be combined with academic research) . Solid experience in pharmacometrics, clinical pharmacology, pharmacokinetics, or a related discipline in a project team setting is preferred, [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Senior Principal Toxicologist-Nonclinical Safety Leader
• Opfikon, Zürich Zuerich
Führungs-/ Leitungspositionen
A leading biotherapeutics company in Zürich, Switzerland is seeking a Principal Toxicologist to develop safety strategies for drug development projects. You will lead the Nonclinical
Expert Team and oversee [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] studies to ensure safety compliance through regulatory submissions. The ideal candidate has a Ph D or DVM in Toxicology or Pharmacology, with 5-8 years of experience in the biotech industry. You will collaborate with cross-functional teams and communicate safety assessments to management. This role offers the opportunity to make a significant difference in patient care. #J-18808-Ljbffr 71753785 [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
• Opfikon, Zürich Zuerich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] implementtoxicology strategiesaligned with clinical development plans. Proactively identify and managesafety risksand 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. Compiletoxicological risk assessmentsfor impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines Stay current with evolvingtoxicology guidelines and risk assessment methodologies. Qualifications and Experience Requirements [. .. ]
Neu Job vor 4 Std. bei Jobleads gefunden
Clinical Evaluation Manager-Freelancer (m/f/d)
• Wien
Freiberuflich
[. .. ] evaluation activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatorycompliant Clinical Evaluation Reports (CERs) to demonstrate device safety and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] performance. You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to postmarket. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practises. Essential skills for your mission: Experience: 1-3 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills Excellent written and verbal communication skills in English Detailoriented with the ability to manage multiple tasks and deadlines Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics Proficiency in [. .. ]
Job gestern bei Jobleads gefunden
Clinical Evaluation Manager-Freelancer (m/f/d)
• Wien
Freiberuflich
[. .. ] activities for my Sugr/ Roche products, including systematic literature reviews, data appraisal, and the authoring of regulatory-compliant Clinical Evaluation Reports (CERs) to demonstrate device safety and performance. [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] You will provide expert medical input to medical risk management and vigilance across the full product lifecycle, from development to post-market. Additionally, you will be responsible for facilitating team backlog grooming and prioritisation of deliverables to ensure efficient, scalable working practices. Essential skills for your mission: Experience: 13 years of experience with regulatory/ CER writing for medical devices or in vitro diagnostics Education: Advanced degree (e. g. , MSc, Ph D, MD, Pharm D, etc) in medicine, life sciences, pharmacology, biomedical engineering, biostatistics/ epidemiology or other related fields Skills and Competencies: Strong analytical and problemsolving skills; Excellent written and verbal communication skills in English; Detailoriented with the ability to manage multiple tasks and deadlines; Capability to make riskbased decisions Technical Proficiency: Basic understanding of clinical research and biostatistics; Proficiency in [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Director Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP)
• Glattbrugg, Zürich
Führungs-/ Leitungspositionen
[. .. ] Description Summary The PK/ QSP Lead is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK) , toxicokinetic (TK) , physiologically-based pharmacokinetic (PBPK) , and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] quantitative systems pharmacology (QSP) modeling strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. Main Responsibilities Strategic Leadership Scientific Expertise Lead the development and execution of integrated PK, PBPK, and QSP modeling strategies across multiple therapeutic programs. Serve as the subject matter expert (SME) in modeling and simulation, advising project teams on optimal study design, dose selection, and risk assessment. Champion model-informed drug development (MIDD) approaches to enhance translational understanding and regulatory confidence. PK and Model Development Lead the design and execution of nonclinical PK and TK studies to support research and [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
• Opfikon, Zürich
Führungs-/ Leitungspositionen
The Senior Director of Nonclinical Toxicology Pharmacokinetics is responsible for overseeing the strategic direction, execution, and integration of nonclinical safety, pharmacokinetics (PK) , and advanced modelingincluding Quantitative Systems
Pharmacology [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] (QSP) to support drug development from discovery through clinical stages across all Therapeutic Areas. This role ensures that all Toxicology and Pharmacokinetic data support regulatory submissions and clinical development and thereby enable effective FIH transition and provide data-driven insights to inform decisionmaking. Strategic Leadership Lead the nonclinical safety and [. .. ] . Ensure compliance with GLP and ICH guidelines for nonclinical studies. Crossfunctional Collaboration Collaborate with relevant R D functions to align Tox/ PK insights and strategies with development goals. Provide expert input into due diligence for inlicensing or partnership opportunities. Collaborate with External Study Management for study execution at CROs. Present findings at internal meetings, scientific conferences, and in peerreviewed publications. Team Leadership Build and mentor a multidisciplinary team of toxicologists, pharmacokineticists, and modelers. Foster a culture of scientific excellence, innovation, [. .. ]
Job vor 13 Tagen bei Jobleads gefunden
Director Translational Sciences (Oncology)
• Mainz, Rheinland- Pfalz
Führungs-/ Leitungspositionen
Jobticket
[. .. ] deep knowledge of and extensive experience with oncology, the role will drive the translational strategies for clinical development of oncology programs based on an integrated view of [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] the respective translational expert functions Responsible for bridging preclinical experimental data to translational strategies in the assigned programs to deeply integrate the mechanism of action to the clinical development plan (target engagement, pharmacodynamics endpoints, patient selection) and correlate with clinical outcomes The role will provide scientific, technologic and strategic guidance and handson contribution to [. .. ] and solve complex problems, experience in collaborating with external specialty laboratories Experience in working within interdisciplinary crossfunctional teams with other key development functions (clinical lead, regulatory, biostatistics, operations and clinical pharmacology) to develop and execute the biomarker strategy in alignment with clinical development objectives Ability to independently drive, manage, execute, and deliver results for a portfolio of complex multifunctional projects Eagerness to work in the dynamic environment of a fastgrowing company and comfortable in working in a matrix environment (global/ crossfunctional) [. .. ]
Job am 14.11.2025 bei Jobleads gefunden
Führungs-/ Leitungspositionen
[. .. ] dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. We are seeking a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Therapeutic Area (TA) Pharmacology Lead (Cardiovascular Renal) to drive the design, execution, and interpretation of invivo pharmacology studies that support drug discovery and development. This role is pivotal in characterising the pharmacological profile of novel therapeutic candidates through internal studies and external collaborations. Main Responsibilities Scientific Leadership Define and lead the nonclinical pharmacology strategy [. .. ] as Sr. Pharmacology lead on TA teams. Work closely with PK, Toxicology, Translational Science, to integrate pharmacology data into broader development plans. Participate in project teams and TAteams and provide expert input on pharmacologyrelated issues. Provide expert input into due diligence for inlicensing or partnership opportunities. Documentation Communication Prepare study reports, presentations, and regulatory documents (e. g. , IND, CTA) . Present findings to internal stakeholders and external collaborators as needed. Team Leadership Lead and mentor a team of Principal and [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
Director, Non-clinical Pharmacology CVR
• Schlieren, Zürich
Führungs-/ Leitungspositionen
[. .. ] dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. We are seeking a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] Therapeutic Area (TA) Pharmacology Lead (Cardiovascular Renal) to drive the design, execution, and interpretation of in vivo pharmacology studies that support drug discovery and development. This role is pivotal in characterising the pharmacological profile of novel therapeutic candidates through internal studies and external collaborations. Main Responsibilities Scientific Leadership Define and lead the nonclinical pharmacology [. .. ] as Sr. Pharmacology lead on TA teams. Work closely with PK, Toxicology, Translational Science, to integrate pharmacology data into broader development plans. Participate in project teams and TAteams and provide expert input on pharmacologyrelated issues. Provide expert input into due diligence for inlicensing or partnership opportunities. Documentation Communication Prepare study reports, presentations, and regulatory documents (e. g. , IND, CTA) . Present findings to internal stakeholders and external collaborators as needed. Team Leadership Lead and mentor a team of Principal and [. .. ]
Job am 13.11.2025 bei Jobleads gefunden
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 internally and externally both in a GLP and non GLP environment. Regulatory Toxicology Role: The Principal Toxicologist will compile Toxicological [. .. ] 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 assessments for impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines. Stay current with evolving toxicology guidelines and risk assessment methodologies. Qualifications [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Director Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP)
• Zürich
Führungs-/ Leitungspositionen
Director Pharmacokinetics (PK) Quantitate Systems
Pharmacology (QSP) page is loaded # # Director Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP) locations: EMEA, CH, Kanton Zurich, Opfikon, CSL Vifortime type: Vollzeitposted [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] on: Heute ausgeschriebenjob requisition id: R-263621CSLs R D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus [. .. ] multiple therapeutic areas. Main Responsibilities:Strategic Leadership Scientific Expertise Lead the development and execution of integrated PK, PBPK, and QSP modeling strategies across multiple therapeutic programs. Serve as the subject matter expert (SME) in modeling and simulation, advising project teams on optimal study design, dose selection, and risk assessment. Champion model-informed drug development (MIDD) approaches to enhance translational understanding and regulatory confidence. PK and Model Development Lead the design and execution of nonclinical PK and TK studies to support research and [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
• München, Bayern
[. .. ] and Country Regulatory Affairs teams. Develop and implement regulatory strategies for registered products, development projects, and new marketing authorisation applications. Stay updated on relevant EU regulations and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] guidelines to provide expert regulatory advice. Represent European Regulatory Affairs on assigned nonproduct related projects. Build and maintain strong relationships with internal and external stakeholders across regulatory and crossfunctional teams. Provide support for regulatory activities in non European countries as needed. Ensure the timely preparation and submission of appropriate documentation for new Marketing Authorisation [. .. ] relevant regulatory authorities. Collaborate as a committed member of the European Regulatory Affairs team, contributing to both functional and crossfunctional projects. Education/ Certificates University graduate in life sciences, preferably pharmacy/ pharmacology. Skills Fluency in written and spoken English is essential, with proficiency in at least one additional European language being highly desirable. Proficient in using regulatory information management systems and tools, including Veeva, Ennov, Power BI, as well as standard office applications such as word processing, spreadsheets, database software, and internetbased [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Director Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP)
• Opfikon, Zürich
Führungs-/ Leitungspositionen
[. .. ] Description Summary The PK/ QSP Lead is responsible for leading the design, execution, and interpretation of pharmacokinetic (PK) , toxicokinetic (TK) , physiologically-based pharmacokinetic (PBPK) , and [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] quantitative systems pharmacology (QSP) modeling strategies to support drug discovery, nonclinical and development programs across multiple therapeutic areas. Main Responsibilities Strategic Leadership Scientific Expertise Lead the development and execution of integrated PK, PBPK, and QSP modeling strategies across multiple therapeutic programs. Serve as the subject matter expert (SME) in modeling and simulation, advising project teams on optimal study design, dose selection, and risk assessment. Champion model-informed drug development (MIDD) approaches to enhance translational understanding and regulatory confidence. PK and Model Development Lead the design and execution of nonclinical PK and TK studies to support research and [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Regulatory Toxicology
• Zürich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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 assessments for impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines Stay current with evolving toxicology guidelines and risk assessment methodologies. Qualifications [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP) - x4 openings
• Glattbrugg, Zürich
Principal Scientist, Pharmacokinetics (PK) Quantitate Systems
Pharmacology (QSP) - x4 openings 1 day ago Be among the first 25 applicants CSLs R D organization is accelerating innovation to deliver [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] greater impact for patients. With a projectled structure and a focus on collaboration, were building a futureready team that thrives in dynamic biotech ecosystems. Joining CSL now means [. .. ] as PK/ ADME/ QSP representative on crossfunctional project teams. Act as Nonclinical Development representative in Research Project teams. Acts as PK Study Monitor for external PK studies. Serves as technical expert for the PK/ QSP organization in the application of advanced PK/ PD, mechanistic, and disease modeling principles and methodologies. Performs advanced PK/ PD modeling utilizing mechanistic and semimechanistic approaches to define the doseconcentrationefficacy/ toxicity relationships, formulate various study design scenarios, and outcome prediction, to inform decision making. Leads study design [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Regulatory Toxicology
• Glattbrugg, Zürich
[. .. ] 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, [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 also compiles toxicological risk assessments across multiple projects, supporting R D, CMC and quality and/or compiling nonclinical [. .. ] 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 assessments for impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines. Stay current with evolving toxicology guidelines and risk assessment methodologies. Qualifications [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Pharmacokinetics (PK) Quantitate Systems Pharmacology (QSP) - x4 openings
• Zürich
[. .. ] PK/ ADME/ QSP representative on cross-functional project teams. Act as Nonclinical Development representative in Research Project teams. Acts as PK Study Monitor for external PK studies. Serves [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] as technical expert for the PK/ QSP organization in the application of advanced PK/ PD, mechanistic, and disease modeling principles and methodologies, Performs advanced PK/ PD modeling utilizing mechanistic and semi-mechanistic approaches to define the dose-concentration-efficacy/ toxicity relationships, formulate various study design scenarios, and outcome prediction, to inform decision making. [. .. ]
Job am 11.11.2025 bei Jobleads gefunden
Principal Scientist, Toxicology
• Zürich
[. .. ] 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] 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 [. .. ] 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 assessments for impurities, extractables and leachables, excipients, and other components in line with ICH, EMA, and FDA guidelines Stay current with evolving toxicology guidelines and risk assessment methodologies. Qualifications [. .. ]
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Häufig gestellte Fragen
Wieviel verdient man als Pharmacology expert pro Jahr?
Als Pharmacology expert verdient man zwischen EUR 70.000,- bis EUR 100.000,- im Jahr.
Wieviele offene Stellenangebote gibt es für Pharmacology Expert Jobs bei unserer Jobsuche?
Aktuell gibt es auf JobRobot 39 offene Stellenanzeigen für Pharmacology Expert Jobs.
Wieviele Unternehmen suchen nach Bewerbern für Pharmacology Expert Jobs?
Aktuell suchen 6 Unternehmen nach Bewerbern für Pharmacology Expert Jobs.
Welche Unternehmen suchen nach Bewerbern für Pharmacology Expert Stellenangebote?
Aktuell suchen zum Beispiel folgende Unternehmen nach Bewerbern für Pharmacology Expert Stellenangebote:
- Roche (1 Job)
- F. Hoffmann- La Roche Gruppe (1 Job)
- F. Hoffmann- La Roche AG (1 Job)
- IQVIA (1 Job)
- Herman Medical Staffing GmbH (1 Job)
In welchen Bundesländern werden die meisten Pharmacology Expert Jobs angeboten?
Die meisten Stellenanzeigen für Pharmacology Expert Jobs werden derzeit in Niedersachsen (8 Jobs), Hessen (2 Jobs) und Sachsen-Anhalt (2 Jobs) angeboten.
Zu welchem Berufsfeld gehören Pharmacology Expert Jobs?
Pharmacology Expert Jobs gehören zum Berufsfeld Pharmazie.
