20 beste Stellen als director, toxicology in kaiseraugst ag – aktuell auf Personalsuche

Director, Toxicology
Swiss Biotech Association —Basel, BS
- Doktorat
- Forschungserfahrung
- Master
Associate Director, Biostatistics
Ironwood Pharmaceuticals —Basel, BS
- Doktorat
- Englisch
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Toxicology Expert
dsm-firmenich —Kaiseraugst, AG
- Doktorat
- Schreibfähigkeiten
- Englisch
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Lonza —Basel, BS
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- Homeoffice
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- Doktorat
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- Führungserfahrung
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Glatt Gruppe —Pratteln, BL
- Teilzeit
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Associate Director, Program and Alliance Management - Discovery to Phase II
Monte Rosa Therapeutics, Inc —Basel, BS
- CHF 145’000 - CHF 170’000 pro Jahr
- 100%
- Doktorat
- Forschungserfahrung
- Microsoft Office
Associate Director, Technical Project Leader Drug Substance
Idorsia Pharmaceuticals Ltd. —Basel, BS
- 100%
- Doktorat
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Neurocrine Bioscience —Allschwil, BL
- 100%
- Management-Erfahrung
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Abbott Laboratories —Basel, BS
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Lonza —Basel, BS
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Director of Operations, Basel
AmaWaterways, LLC —Basel, BS
- 100%
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BeiGene —Basel, BS
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Director Global Communications
Jet Aviation —Basel, BS
- Schreibfähigkeiten
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Regional Director, Engineering - Clinical Trials
Thermo Fisher Scientific —Allschwil, BL
- 100%
- Bis zu 50% Reiseanteil
- PMP
- Master
2 Tage

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Director, Toxicology

Swiss Biotech Association
Basel, BS

Jetzt bewerben

Details zur Stelle

Qualifikationen

Doktorat
Forschungserfahrung
Master
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

Director / Associate Director – Toxicology

Location: Basel

Monte Rosa Therapeutics is searching for a Toxicology Lead to direct nonclinical safety and toxicology work for programs to enable drug candidates from discovery through development. This position will lead and develop nonclinical toxicology strategies to support Monte Rosa’s diverse drug candidates during all phases of development. The Toxicology Lead will contribute to the R&D strategy and implement the strategy and will report to the Senior Director of Nonclinical Development. This is an individual contributor role by designing, conducting or overseeing studies, analyze/interpret, and report in vitro, ex vivo, and in vivo non-GLP (or GLP studies conducted at CROs) nonclinical pharmacology, PK/PD, and/or toxicology studies, in collaboration with study monitors and other scientists. Ensure appropriate quality of documentation and record keeping.

The Lead scientist will support global regulatory activities related to nonclinical sections of filings including INDs, IBs, and annual reports. The discovery toxicologist interacts directly with multidisciplinary teams including biology, medicinal chemistry, DMPK, clinical science, and outside CRO’s in research and/or development projects to move discovery candidates into development. Introduction and growth into regulatory toxicology will be an extension of this position. The ideal candidate will be able to help evolve Monte Rosa’s hit identification and hit-to-lead endeavors through embracing novel assay technologies, enhancing overall process and actively drive internal and external partnerships.

Principal Duties and Responsibilities

1. Develop Toxicology studies for Molecular Glue Degraders by bridging Monte Rosa’s platform to aid in the understanding/minimizing of potential issues.

2. Work cross functionally and culturally with departments on in vitro and in vivo models, weaving in toxicological datapoints to help mitigate findings.

Participate in the design of early in vitro toxicity screening and/or secondary/safety pharmacology studies for small molecules in various stages of preclinical research and development. Implement and manage studies with CRO and/or academic collaborators.
Execute studies designed to address mechanistic issues and/or unpredicted adverse findings in preclinical and/or clinical trials and provide results on a timely basis to support the ongoing project teams and leadership team.
Select CROs and represent Monte Rosa as the Study Monitor for various in vitro and in vivo toxicology studies.
Responsible for protocol design and reviewing protocol amendments.
Review all experimental data and ensure timely delivery of toxicology reports that may be used for regulatory submissions and assist in the preparation of safety pharmacology and toxicology sections for Investigational New Drugs (INDs), annual reports, Investor Brochures (IBs) and New Drug Applications (NDAs).
Knowledge, Skills, and Ability

PhD degree or DVM & 5 yrs of scientific experience OR Master’s degree & 10 years of scientific experience in preclinical toxicology and drug development in the pharmaceutical/biotechnology sector; DABT preferred

Familiarity with GLP regulations and ICH/FDA guidelines for the conduct of toxicology studies to support regulatory filings

Experience working with Contract Research Organizations

Ability to develop and deliver clear and concise presentations for both internal and external meetings

Outstanding written and verbal communication skills

Interested candidates should forward a resume and cover letter via our website, Monte Rosa Therapeutics - Careers

www.monterosatx.com

Monte Rosa Therapeutics rational approach in targeting disease-causing proteins for degradation will deliver pioneering therapies for cancer and other diseases. Delivering this new generation of treatments to the patients requires a conceptual change. Monte Rosa recognizes this urgent need and is missioned to develop innovative protein degraders as a solution. Combining deep knowledge, insight and leading-edge science, our integrated engine is built for that purpose

Company

Monte Rosa Therapeutics AG

Location

Basel, Switzerland

Type of job

Research

Contact information

HR
[email protected]

Jetzt bewerben

Erweiterte Suche

director, toxicology Jobs in kaiseraugst ag

Director, Toxicology

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Toxicology Expert

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Director, Clinical Development

Head of Digitalization & CSV (m/w/d)

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Associate Director, Technology Transfer 80-100%

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Director of Operations, Basel

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Director Global Communications

Regional Director, Engineering - Clinical Trials

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