As a leading Contract Research Organization (CRO), we partner with pharmaceutical, biotechnology, and life science companies to advance the development of novel therapeutics. Our Developmental & Reproductive Toxicology (DART) team supports regulatory nonclinical studies that evaluate potential effects on fertility, embryo-fetal development, and pre/postnatal development. We are seeking a Study Supervisor who is passionate about animal welfare, operational excellence, and scientific rigor to support critical studies that help bring life-changing therapies to patients worldwide. The DART Animal Research Study Supervisor provides technical and operational support for regulated DART studies conducted in compliance with Good Laboratory Practice (GLP) regulations, study protocols, and institutional animal care standards. This position performs specialized animal procedures, reproductive assessments, study observations, biological sample collection, and data recording while ensuring the highest standards of animal welfare and scientific integrity. The successful candidate must be able to work in a fast-paced CRO environment supporting multiple studies, and timelines simultaneously.
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED