Senior Toxicology Scientist – Nonclinical Safety & INDs

Monte Rosa Therapeutics; Basel; Vor Ort; CHF 150.000 - 210.000; Vollzeit

Zusammenfassung

Monte Rosa Therapeutics in Basel seeks a toxicologist to direct nonclinical safety and toxicology for programs through discovery to development. This individual contributor role will work with Senior Director of Nonclinical Development to design and oversee studies and interpret results, ensuring documentation quality.

The ideal candidate has a PhD or DVM with 5+ years in preclinical toxicology or, alternatively, a Master’s with 10+ years.

Qualifikationen

• Requires advanced degree and significant experience in preclinical toxicology.
• Experience with GLP, ICH, OECD guidelines and regulatory filings.
• Ability to design and interpret nonclinical studies.

Aufgaben

• Lead nonclinical safety and toxicology studies from discovery through development.
• Design, conduct, or oversee in silico/in vitro/in vivo studies, GLP and non-GLP.
• Coordinate with CROs and internal teams; ensure quality documentation.
• Support regulatory filings (INDs, IBs, NDAs) and safety sections.
• Present data clearly to internal and external stakeholders.

Kenntnisse

Excellent communication skills

CRO management

Regulatory toxicology knowledge

Independent contributor

Ausbildung

PhD or DVM in toxicology or related field

Master’s degree in toxicology or related field

Tools

CRO oversight experience

Jobbeschreibung

Monte Rosa Therapeutics in Basel seeks a toxicologist to direct nonclinical safety and toxicology for programs through discovery to development. This individual contributor role will work with Senior Director of Nonclinical Development to design and oversee studies and interpret results, ensuring documentation quality.

The ideal candidate has a PhD or DVM with 5+ years in preclinical toxicology or, alternatively, a Master’s with 10+ years.