Sole project support associate on 4 Phase III and 1 Phase II inflammation clinical trials.Track and manage site selection, clinical trial management system, and eTMF updates.Ensure proper review on monitoring visit reports, monthly regulatory documents updates, and data listings.Interact and communicate with external vendors to ensure a seamless flow of information between vendors and study teams. Support vendor, region, and global leads with site selection, investigator updates, and regulatory document updates.Ensure study teams are inspection ready through continuously staying up to date with changes that occur with sites, investigators, and vendors.

Support data driven decision making across all therapeutic areas within Clinical Development Operations.Develop insights and analytical business solutions from data to respective stakeholders.Communicate cross functionally to deliver insights.

Developed business process to streamline approach to when method variability occurs in QC lab testing. Developed custom reports for Waters Empower 3.

Studied the development of a working glaucoma model in mice and rats.Experimented with dosage of antibodies necessary for clear results by performing immunohistochemistry staining studies on the retina.Modeled retinopathy of prematurity in oxygen induced retinopathy mice.