Preclinical Research Associate

Key responsibilities: Conduct quality control reviews of nonclinical content for DMPK and Toxicology reports Edit and format regulatory submission documents to ensure compliance with style guides and guidelines Support literature reference activities, including retrieval and upload to electronic document management systemsRequired qualificationsBachelor's degree in Life Sciences with 3 to 4+ years of relevant experience In-depth knowledge of Good Laboratory Practices, FDA regulations, and ICH guidelines Proven ability to manage multiple projects in a fast-paced environment Proficiency in Microsoft Suite; experience with Veeva preferred Experience with regulatory submissions is a plus