Job description
**Job Title: Preclinical Study Manager**
The Preclinical Study Manager directs the operational aspects of toxicology studies, both non-GLP and GLP, acting as the main point of contact between our organization and contract research organizations. This role is pivotal in ensuring that scientific goals are achieved, study deadlines are adhered to, and regulatory standards are consistently met throughout the drug development journey. Applicants should hold a Bachelor’s degree in a scientific discipline along with a minimum of 5 years of pertinent experience within the biotech, pharmaceutical, or contract research organization environments. A strong understanding of GLP regulations, ICH/FDA guidelines, and excellent communication skills for effective collaboration across various teams are essential.
Revolution Medicines provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
