Descripción de la oferta
ToxicologistSi sus habilidades, experiencia y cualificaciones coinciden con las de esta descripción del puesto, no demore su solicitud.ToxicologistToxicologist with a Ph.D. in relevant area and extensive experience in preclinical (in vivo) drug efficacy and toxicology studies.A company born from innovation and the desire to offer the highest quality to everyone.We are seeking a highly qualified Senior Toxicologist with a Ph.D. in Pharmacology or another relevant biomedical discipline and extensive experience in preclinical toxicological assessment of drugs. The ideal candidate will have a solid scientific and biomedical background, be familiar with ICH/OECD regulatory guidelines, and possess expertise in toxicology screening strategies, study design, data interpretation, and human translation of toxicological findings in the context of drug development. This role is suited for someone motivated to contribute to the development of safe medicines for patients in need through strategic and scientific guidance to project teams .Prepare and review toxicology‐related study protocols, reports, and regulatory documents in compliance with SOPs, GLP regulations, and ICH/OECD guidelines.Advise the team on all aspects of the toxicological profile of potential candidate drugs and drugs under development, including toxicology screening strategy, experimental study designs, scientific queries, interpretation of study findings, and translation strategy to humans.Provide strategic toxicology input as a core member of project teams, ensuring alignment of toxicology plans with overall development objectives.Partner with internal stakeholders and CROs to support the design, conduct and scientific oversight of preclinical toxicology studies in collaboration with other team members .Analyze, interpret, and review toxicology data, generating high-quality and accurate assessments.Experience with new approach methodologies (NAMs), including in vitro and alternative models to support toxicology screening and mechanistic understanding.Familiarity with integrating in vitro and in vivo data into overall non‐clinical safety packages and regulatory submissions.5-10 years of experience in preclinical drug toxicology studies (GLP and non-GLP) and translation to humans. xcskxlj ~ Proven scientific writing and communication skills.~ Experience in project management~ Professional proficiency in EnglishPermanent contractHealth insurance - flexible coverageProfessional development opportunities
