 Managed day-to-day operations of Furosemide Max PK study as well as the close-out activities for the Furosemide phototoxicity, photoallergy, and sensitization studies Initiated and executed perspective site searches for Furosemide Phase III program in order to find the most qualified research sites and doctors  Tasked with on-site monitoring the dermal safety and Max PK studies for Cutanea’s Furosemide program Built and maintained relationships by attending Site Initiation Visits as a sponsor representative to ensure adequate performance by Contract Research Organization monitors Performed oversight and management activities with monitoring vendors for Non-IND and early development studies Carried out remote monitoring tasks for both the Omiganan Rosacea and Furosemide Common Warts pivotal Phase III Programs including Adverse Event and Discontinuation tracking Accounted for completion of literature reviews and protocol synopses for new perspective studies in Actinic Keratosis and Seborrheic Dermatitis within Cutanea’s Early Concept Development Committee Successfully completed multiple revisions and quality control of Investigator’s Brochures, Drug Safety Update Reports and Study Protocols

- Collaborated with multiple departments on a drug development team- Created comprehensive vendor profiles for packaging options intended for a drug currently in development- Compiled and analyzed two years of batch stability data to ensure no problems were occurring with a particular drug- Developed strong skills in professional correspondence and business etiquette

- Managed projects from start to finish- Displayed good leadership and business skills in making sure jobs were done efficiently and in the most cost effective manner- Developed strong personal skills in dealing with clients and homeowners on a daily basis- Specialized in the design and construction of sidewalks, retaining walls, patios and sea walls from stone products