Overview:
In this role you will lead preclinical rodent toxicology studies and ensure high-quality data to support discovery and early development. You will work closely with scientists and Study Directors to plan, execute, and document in-life toxicology activities. You will uphold regulatory and company standards while advancing SOPs and lab operations. This position offers opportunities to grow into people management and to contribute to a collaborative, impact-driven team. You will help shape studies that enable science-driven decisions at scale. Compensation / Benefits performance-based cash incentive eligibility for annual equity awards comprehensive benefits package 401(k) with company contribution and match generous time off package salary range disclosed
Responsibilities:
Lead and support preclinical rodent toxicology studies and manage study logistics Contribute to lab meetings, draft study protocols with the Study Director, and schedule activities Perform technical procedures: animal handling, article administration (PO, IV, SC, IP, etc.), clinical monitoring, and sample collection and processing Ensure meticulous documentation and data review; maintain compliance with policies and SOPs, including IACUC and regulatory requirements Contribute to updating SOPs and working instructions as needed Demonstrate excellent laboratory citizenship; work independently and collaboratively to maintain a productive team environment Potential to develop into a people manager
Key requirements:
Bachelor of Science in Biological sciences Over 10 years of experience in preclinical toxicology Experience in Big Pharma, CRO or Biotech Experience (or ability to learn) using in-life data acquisition systems Must work some weekend days every month Dual level posting; final level determined by hiring team collaboration independence with teamwork clear communication animal handling and care administration of test articles via multiple routes clinical monitoring and sample collection