Experienced pharmaceutical professional with a proven track record of driving successful drug development initiatives through advanced modeling and simulation techniques. I bring over a decade of expertise in impactful training and cross-functional collaboration, ensuring compliance with regulatory standards and achieving strategic objectives. My passion lies in optimizing operational efficiency and guiding transformative initiatives in the pharmaceutical sector. I am dedicated to leveraging my wealth of experience to provide drug development, training, and project management consulting services. If you're seeking a seasoned consultant to drive your projects to success, let's connect and explore how I can contribute to your organization's growth and excellence.

I personally craft bespoke travel experiences for our clients by applying a meticulous, research-driven approach to travel planning, blending the precision of science with the art of creating memorable and personalized journeys.Travel Planning and Consultation: Personally design customized travel itineraries that meet the diverse needs and preferences of our clients. From luxury escapes and adventure tours to cultural explorations and family vacations, I ensure each trip is tailored to provide an unparalleled experience.Client Relationship Management: Build and maintain strong, trust-based relationships with clients, understanding their travel aspirations and preferences to deliver services that exceed expectations. My role involves being an accessible and knowledgeable point of contact for clients before, during, and after their travels.

Designed, coordinated, and delivered PBBM/PBPK modeling and simulation training both internally and externally. Developed, outlined, and executed the strategic vision and expansion of a PBBM/PBPK training team. Built and reviewed PBBM/PBPK models for training material. Coached and mentored scientists to help them become experienced PBBM/PBPK modeling and simulation trainers. Discussed PBBM/PBPK modeling and simulation training and strategy with clients. Served as a technical mentor during software evaluations to ensure uptake of the tools. Served as an application scientist, performing PBBM/PBPK modeling and simulation to address objectives with client projects, including, but not limited to, FIH predictions, formulation design/optimization, population simulations, special populations, disease state modeling, and DDI predictions. **Professional Highlights:**🎯 LMS Implementation: Successfully led the implementation of a corporate-wide Learning Management System, ensuring alignment with schedule and budget constraints.📚 Adult Learning Expertise: Trained over 500 external clients year-over-year, implementing adult learning principles and strategically interfacing with Business Development, Operations, and Subject Matter Experts (SMEs) for data-driven training outcomes.🏢 Training Department Establishment: Orchestrated the establishment of a training department within a year, ensuring organizational learning needs were effectively met and streamlined workshops and innovative offerings.🤝 Strategic Guidance: Provided valuable insights as an executive team member, guiding strategic divisional goals with a focus on operational efficiency.

Collaborated with clients to strategically plan and execute analyses during the drug development process. Performed clinical pharmacokinetic (PK) analysis and interpret clinical PK studies using NCA, developed and validated clinical population PK and PK-PD models using NONMEM, performed mechanistic absorption and physiologically-based pharmacokinetic (PBPK) analyses using GastroPlus.**Professional Highlights:**📋 Regulatory Contributions: Substantively contributed to regulatory submissions, including a BLA and multiple pediatric labeling updates, demonstrating a strong understanding of FDA, EMA, and PMDA guidelines.🤝 Strategic Guidance: Provided valuable insights as an executive team member, guiding strategic divisional goals with a focus on operational efficiency.

Collaborate with clients to strategically plan and execute analyses during the drug development process. Perform clinical pharmacokinetic (PK) analysis and interpret clinical PK studies using NCA, develop and validate clinical population PK and PK-PD models using NONMEM, perform mechanistic absorption and physiologically-based pharmacokinetic (PBPK) analyses using GastroPlus.

Act as principal investigator on internal and external preclinical and clinical studies. Responsible for carrying out PK analysis of preclinical and clinical pharmacokinetics, bioavailability, bioequivalence, and Population PK studies.

Perform population pharmacokinetic analysis of an antiprogestin for the treatment of endometriosis and uterine fibroids.

Clinical Pharmacokinetics (046:170)LectureGrade ExamsMaintain course website

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