• Successfully leads multiple time-sensitive projects from pre-clinical development through clinical Phase I/II, contributing to over $5M in recognizable revenue.• Devised and implemented a cost-saving initiative valued at over $1M per year by reducing outsource costs.• Utilizes project management tools such as MS Projects, Smartsheet, and Workfront.• Represents the firm as a liaison at conferences and events to source potential clients and/or strategic partners.• Drives revenue-generation and growth through ensuring successful and timely contract completion while demonstrating a client-centric mentality.• Stays current with innovations and advancements in emerging industry trends.• Works jointly with Business Development (BD) to write technical proposals for prospective clients.• Ensures departmental budgets align with current and forecasted financials.• Coordinates meetings with clients and cross-functional teams to provide project updates and align expectations in forthcoming tasks.• Performs all activities in compliance with cGMP standards and FDA regulations.• Develops robust drug formulations and analytical chemistry methods.• Writes concise technical reports for drug product pre-clinical development.•Generates and executes method validations and qualifications (i.e., IQ/OQ/PQ).

• Organized and maintained GMP-compliant materials and equipment through utilizing tools such as Microsoft Excel, Smartsheet, and Qualer.• Generated quality and regulatory documentation compliant with FDA regulations and cGMP standards.• Developed and executed analytical method validation protocols.• Maintained accurate, organized, and detailed cGMP- compliant documentation.

• Successfully synthesized novel compounds.• Applied advanced chemical knowledge and critical thinking skills.• Analyzed and characterized products via LC-MS and NMR.• Presented experimental findings and future directions to • Performed extremely sensitive reactions with precision.• Ensured reagents, glassware, and equipment were properly maintained.