Claire Sipes

Identified discrepancies between federal regulations and internal SOPs for specimen retention and collaborated to clarify and align internal procedures with compliance standards. • Reviewed and quality-controlled IND/NDA pharmacology and toxicology documentation for regulatory submission, ensuring data integrity and compliance. • Managed international CRO communications supporting in vivo pharmacology studies. • Created and delivered company-wide Business Review on AI in nonclinical safety to 30+ colleagues. • Uploaded 90+ reports into Veeva Vault to support NDA/IND Submissions. • Built 20 Excel trackers (e.g., Sample Retention Tracker, ToxApp Dashboard, Master Report Document, DMPK Study List) to organize large experimental datasets and study documentation. • Built custom GPT leveraging AI to assist in preliminary bioanalytical data review.

-Delivered excellent customer service in a fast-paced environment.

-Conducted experiments in neuroscience, utilizing Prism for data analysis. -Performed laboratory techniques such as fly husbandry and larval dissections. -Supported the lab’s mission to uncover insights into role of glia on seizure susceptibility.

-Taught various subjects across grade levels, adapting to classroom needs. -Encouraged engagement through clear explanations and interactive learning.

-Provided one-on-one and group tutoring to middle-school STEM students. -Simplified complex topics to improve academic performance and confidence.