Preclinical Research Associate

Performs quality control (QC) review of nonclinical content for various DMPK and Toxicology reports as well as Module 2, Module 4 of regulatory submission documents.Provides editing, word formatting, and PDF submission-readiness support for nonclinical regulatory submission documents in alignment with style guides and regulatory guidelines.Provides Veeva support for various nonclinical regulatory document lifecycle management activities.Supports literature reference-related activities, including (but not limited to), retrieval, copyright clearance review, upload to electronic document management system, etc.Independently solve problems, exercising sound judgment, appropriate interfacing, and flexibility within a dynamic environment.