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Postdoctoral scientist in Dr. Onohara’s laboratory at Nationwide Children’s Hospital and clinically trained cardiovascular surgeon with over ten years of experience in valvular heart disease and heart failure. My research focuses on translational cardiovascular device development for advanced ischemic heart failure and functional mitral regurgitation, with particular emphasis on minimally invasive ventricular reshaping therapy. I have hands-on experience in large-animal cardiovascular surgery, chronic swine models of ischemic cardiomyopathy, transapical device implantation, echocardiographic assessment, invasive pressure-volume loop analysis, and tissue-level evaluation of myocardial remodeling. Since joining Dr. Onohara’s laboratory in 2024, I have dedicated my work to developing and evaluating a left ventricular reshaping device in a six-month post-infarction swine model of advanced heart failure. My long-term goal is to become an independent physician-scientist, integrating clinical cardiovascular surgery with translational research to develop less invasive and more effective therapies for valvular disease and heart failure.

Security professional with 7+ years of experience in investigations, risk analysis, and operational security across corporate and military environments. U.S. Army veteran with active Secret Clearance and current experience in a Global Security Operations Center (GSOC) while finishing a Master of Public Administration in Disaster Management. Proven ability to conduct investigations, analyze incidents, and support loss prevention strategies. Strong background in security operations, incident response, intelligence assessment and analysis, and cross-functional coordination to mitigate risk and protect assets.

Professional military candidate with track record of success in high-stakes environments. Skilled in tactical operations, strategic planning, and leadership. Strong focus on team collaboration and mission accomplishment. Reliable and adaptable, with expertise in weapons handling, physical fitness, and situational awareness.
Organized and detail-oriented Investigator dedicated to improving efficiency, productivity and profitability through continuous process improvement. Analytical thinker skilled at developing innovative solutions to complex problems.

Experienced and licensed Pharmacist with a Master's degree in Pharmacy, specializing in Quality Assurance, and over 8 years of versatile expertise in pharmaceutical and biotech domains. Certified Scrum Master and adept leader known for driving revenue growth, fostering client relationships, and leading cross-functional teams. Eager to spearhead the development, implementation, and management of quality systems as Director or associate Director roles. Committed to ensuring regulatory compliance and fostering a culture of continuous improvement for organizational success

 Dynamic and results-driven Analytical Leader with over 20 years of extensive experience in pharmaceutical analytical research, method development, validation, regulatory submissions, and quality systems. Expertise includes aligning laboratory operations with GMP, GLP, OQM, HSE, ISEC, and Quality Guidelines while fostering a culture of compliance, safety, and continuous improvement. Proven track record in building and mentoring high-performing teams, streamlining processes, and delivering innovative analytical solutions that expedite product development and regulatory approvals. Comprehensive hands-on proficiency spans analytical testing across various formulations, including Active Pharmaceutical Ingredients (APIs), Solid Oral Dosage Forms (OSDs), and Parenteral Liquid Injections (LIVI), complemented by a strong foundation in stability studies, technology transfers, compliance, audit readiness, CAPA management, documentation optimization, and team leadership. 

Strategic biopharmaceutical leader with 10+ years of experience and deep technical expertise in analytical method development, including HPLC, UPLC, CE-SDS analysis, qPCR, ddPCR, Potency, TCID50, ELISA, Octet (BLI), AUC, and a broad range of analytical methods for process and product characterization. Proven track record in method development, transfers, and validation with technical excellence, and leading cross-functional collaborations working with CDMO/CRO/CTO. Adept at driving biologics & gene therapy programs from development to clinical stages. Recognized for leadership, analytical problem-solving, team management and authoring IND/CTA/BLA documentation and relevant CMC sections.

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