novartisSomerville, MA
• In-Vivo Translational Toxicology Scientist, Principal Scientist I or II
• In-Vivo Translational Toxicology Scientist, Principal Scientist I or II
• In-Vivo Translational Toxicology Scientist, Principal Scientist I or II
novartisSomerville, MA
today
Medical Scientists, Except EpidemiologistsBiological Scientists, All OtherLife Scientists, All Other
Research and Development in BiotechnologyResearch and Development in the Physical, Engineering, and Life SciencesBiological Product Manufacturing
Apply for this role (opens in a new tab)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
Also on the board Same function, level within a rung
Level
Mid
Location
Somerville, MA
Occupation
Medical Scientists, Except Epidemiologists
Industry
Research and Development in Biotechnology
Posted
today