3 Jobs für Clinical Drug Toxicologist
Stellenangebote Clinical Drug Toxicologist Jobs
Job vor 8 Tagen bei Jobleads gefunden
• Lausanne, Waadt
Führungs-/ Leitungspositionen
[. .. ] a central role in ensuring the continuation and ongoing development of robust and accountable science behind our Health and Wellness portfolio. The successful candidate will bring a [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] strong understanding of drug development and the commercialization processes alongside a good knowledge of the regulatory environment and experience in overseeing or conducting pre-clinical studies. In addition a proven understanding of study design and methodology and the ability to balance safety and efficacy aspects will be required. Working across a wide spectrum encompassing supplier evaluation and qualification, materials science and product development, this role is part of a global team but will be required [. .. ] testing Previous pharmaceutical or biopharmaceutical industry experience is of significant benefit. Academic degree in life sciences (pharmacy, biochemistry, medicine, biology, veterinary) , with preferably specialization in toxicology (Certified European Registered Toxicologist (ERT) or equivalent) . Proven Industrial experience in toxicological (risk) assessments of natural products or biopharmaceuticals Demonstrable experience in overseeing or conducting preclinical studies, including studies to investigate the pharmacodynamic, mutagenic/ genotoxic and carcinogenic properties Understanding of drug development and commercialization processes; knowledge of the regulatory environment; experience in overseeing [. .. ]
Job vor 10 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 [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] deep expertise in drug development, regulatory frameworks, and preclinical study oversight, balancing safety and efficacy considerations. Responsibilities Prepare complex toxicological risk and hazard assessments for innovative botanical drugs and consumer products, including ADE/ PDE determination and safety risk evaluation using invitro, invivo, and insilico approaches. Interpret preclinical studies to assess safety pharmacology, mutagenic/ genotoxic, [. .. ] 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. Qualifications 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 am 24.04.2026 bei Jobleads gefunden
• München, Bayern
We are seeking a talented and motivated Safety
Toxicologist to join a growing nonclinical safety team in Munich. This is an exciting opportunity to contribute to the development of innovative [...]
MEHR INFOS ZUM STELLENANGEBOT
[...] therapies within a collaborative and sciencedriven environment. As a Safety Toxicologist, you will support the design, monitoring, and interpretation of nonclinical toxicology studies across a diverse pipeline of drug candidates. You will work closely with crossfunctional teams to ensure that safety assessments are robust, scientifically sound, and aligned with regulatory expectations. Key Responsibilities: Design and oversee nonclinical toxicology studies (GLP and non GLP) to support drug development programs Interpret toxicological data and contribute to safety risk assessments and mitigation strategies Prepare and review regulatory documents (IND, CTA, NDA modules) Collaborate with pharmacology, DMPK, clinical, and regulatory teams Manage external CROs to ensure highquality study conduct and timely delivery Contribute to the development of safety strategies across multiple projects What youll need: Ph D, DVM, Pharm D, or MSc with significant experience in toxicology or a related discipline Experience in nonclinical safety/ toxicology within pharma, biotech, or [. .. ]
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 3 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 Bayern (1 Jobs), Nordrhein-Westfalen (0 Jobs) und Baden-Württemberg (0 Jobs) angeboten.
Zu welchem Berufsfeld gehören Clinical Drug Toxicologist Jobs?
Clinical Drug Toxicologist Jobs gehören zum Berufsfeld Pharmazie.
