Senior Manager or Associate Director, Preclinical Safety Study Monitor

Role: Senior Manager/Associate Director, Preclinical Safety Study Monitor at Kymera, overseeing outsourced nonclinical toxicology studies to support drug development. Responsibilities include acting as the scientific and operational liaison with CROs, developing and reviewing study protocols, monitoring study conduct through site visits and data reviews, ensuring high-quality and compliant execution, and authoring or reviewing toxicology reports. The role entails coordinating with cross-functional teams (DMPK, Bioanalytical, CMC), managing study timelines, and escalating issues as needed. Qualifications: Bachelor's or Master's in Toxicology, Pharmacology, Biology, or related field; 7+ years supporting nonclinical safety studies, including 3+ years monitoring GLP toxicology at CROs; strong knowledge of GLP regulations, study design, and regulatory standards; excellent communication and organizational skills; willingness to travel 5-10%. HighValue: Support for nonclinical safety in biopharma drug development, with focus on GLP toxicology studies, in support of innovative therapeutics, likely biologics or small molecules, in preclinical or early clinical stages. Collaboration with cross-disciplinary teams and external CROs is essential. WorkSetup: flexible travel, situated within the company's preclinical safety organization.