Statistical and Data Science consulting for Clinical Trials and Real World EvidenceProvide business case and project management planning for analytics product companiesProvide strategic roadmap input for startups in the data science and AI sectorsConduct ad-hoc data analysis and predictive analytics on NIH-funded studies in OncologyAssist a Professional Sports Franchise with creating a scalable data and analytics platform

Support Real World Data Solutions for Top 50 Biopharma including data insights and actionable insights for Oncology pipelinesDrive strategy for Digital Clinical Trials initiative in partnership with Biopharma and a large US based Oncology care and research network Collaborate closely with potential Provider networks to create and integrate novel software for use at clinical research sites for Patient Recruitment and RetentionBlend clinical trial data with Real World Data to promote harmonization of Oncology specific data strategies in large BioPharmaContribute to innovative and new statistical, machine learning and AI methods development for technology product enhancementsDrive adoption of real world data and technology offerings across biopharma portfolios in OncologyCreate the strategy and operational execution plan required for Certification, Enablement, Delivery and Training of a Real World Data technology platform to Oncology BiopharmaDrive growth of strategic partnerships in the clinical research and technology spaceContribute subject matter expertise to Go-To-Market and other marketing initiatives

Lead the first Strategic Data Science group for Real World Data Oncology solutionsDrive the adoption of real world data at large BioPharma organizationsGuide predictive model development aligned to strategic portfolio needs at large BioPharma organizationsLead and guide analysis relevant to the RWE strategy in Oncology indicationsConsult with BioPharma clients on optimal usage of real world data in the context of ConcertAI offeringsBlend clinical trial data with Real World Data to promote harmonization of Oncology specific data strategies in large BioPharmaPerform User enablement program including formal trainings and 1-on-1 consultingProvide internal teams feedback and new use cases for integration into ConcertAI offerings

Cambridge Semantics Inc. is an enterprise Big Data Management and Exploratory Analytics software company.▬▬▬▬▬▬▬▬▬▬▬▬▬As a member of the executive leadership team at Cambridge Semantics, I develop and enhance the company’s initiatives in Biopharma and Healthcare — providing go-to-market strategy, thought leadership, and innovative solutions in data science applications.A Senior Analytics & Data Science professional, I promote and strengthen the company’s vision in the areas of clinical development, real world evidence, and data science in helping provide our customers with an open standards based semantic layer along with an enterprise scale information fabric as an overlay that manages common access to all of their organization’s information assets. Comprehensive areas of focus include:♦ Helping Biopharma and Healthcare customers show the value of their Hadoop/Data Lake investments♦ Delivering strategies in Market Positioning of Semantic Graph Database (Anzo Smart Data Lake 4.0) technology to Pharmaceutical and Healthcare customers♦ Connecting Data Science applications to Semantic Graph Database concepts♦ Supporting marketing events and various thought leadership activities Connect with me for more information about the full extent of services from Cambridge Semantics.

PerkinElmer’s Informatics solutions and specialized scientific know-how empower customers to gain critical insights from their data analytics and accelerate informed decisions.▬▬▬▬▬▬▬▬▬▬▬▬▬Leading the design and implementation of Real World Data & Analytics solutions, I drive our Go-To-Market strategy and identify innovative opportunities for growth. As the Director – Real World Evidence & Data Science, I am a thought leader, bringing in-depth technical knowledge combined with strategic business leadership to propel PerkinElmer’s company goals.Since beginning this role, have been given the added responsibility of leading the Global Marketing Strategy for PerkinElmer’s Data Science products (namely Tibco Spotfire), owning a portfolio that had gross global revenues of $25+M USD annually. Executive communication of launch plans for any new product initiatives. Track monthly and quarterly sales metrics (financials and lead generation-to-conversion). Evaluate and provide strategic input for Product, Promotion, Placement, and Pricing.Areas of Focus Include: Advanced Analytics & Machine Learning, Client Relationships, Public Speaking, Team Leadership, Business Development, Strategic Planning, Sales Enablement, Reporting, Research.Key Highlights:♦ Providing strategic guidance on solution building and user adoption ⇨ managing company initiatives as the intermediary consultant between groups within a customer account (e.g., epidemiology and IT) ♦ Delivering public speaking engagements for notable industry events ⇨ including the IE Big Data and Analytics in Pharma (June 2017) and Global Artificial Intelligence Conference (October 2017)♦ Crafting product/solution messaging and positioning ⇨ including in Real Word Evidence, Health Economics, Outcomes, & Observational research♦ Leading business development by identifying key opportunities within current and new customer accounts ⇨ acting as a Trusted Advisor, Thought Leader, and Cross-Functional Manager

SAS is the leader in analytics. Through innovative analytics, business intelligence and data management software and services, SAS helps customers at more than 83,000 sites make better decisions faster.▬▬▬▬▬▬▬▬▬▬▬▬▬As the Principal Consultant & Practice Lead for Health & Life Sciences for SAS, I served as the Lead Consultant on the practice of data science in Life Sciences/BioPharma. This was a Thought Leadership role within the sector for Business Development and Marketing of SAS solutions. Here, I provided personalized solutions for our Life Sciences/BioPharma Customers on Enterprise Solution strategies in alignment with company business goals. After a successful first 18 months on the job, I progressed from Senior Consultant to overall Principal and Practice Lead. Areas of Sales Support & Enablement include: Real-World Evidence, Health Economics and Outcomes Research, Clinical Trial Optimization, and Risk-based monitoring.Additional Achievements:♦ Delivered innovative solutions with machine learning & predictive analytics ⇨ enhancing clinical and commercial use cases in Biopharma♦ Selected as Media Representative during Zika Virus media interest escalation ⇨ providing information on predictive analysis and its power to deliver solutions worldwide* ♦ Delivered Public Speaking Engagements at industry events ⇨ including EyeforPharma RWE - “Quantifying the Patient Journey: foundations for Real World Evidence”♦ Developed and delivered external marketing content SME for Life Sciences/BioPharma solutions ♦ Led product strategy and early software prototyping activities in support of SAS’ entrance into the Real World Evidence solution space. ♦ Helped formulate partnerships with other domain-specific consultancies to sell solutions in the RWE space together

IQVIA explores Human Data Science — unleashing the power of data science and human science to improve health outcomes.▬▬▬▬▬▬▬▬▬▬▬▬▬As the Director for Predictive Analytics, I held a leadership role within our dedicated Innovation unit. Areas of Focus include: IT Management, Growth Strategy, Mentoring, Project Management, Training & Development, and Team LeadershipA primary responsibility in this role — Product Owner of custom-built Clinical Trial predictive analytics suite. This included: global feasibility module, global site start-up simulation, probabilistic and deterministic models, global patient recruitment simulation and probabilistic models, and a real-world data explorer. I founded and was instrumental in creating the vision and strategy for the company’s first group of this type and left as Director.Prior to my role as Director, I provided team leadership and assisted in strengthening strategic stakeholder relationships as the Assistant Director of Predictive Analytics. Additional Highlights:♦ Led expansion of expansion of predictive analytics software influence (internal/external) ⇨ payer/provider and cost-benefit analysis in value-based drug development♦ Selected to perform an advisory role for predictive models in large cardiovascular outcome studies ♦ Provided leadership for direct reports and junior staff members ⇨ including mentoring and coaching♦ Created an analytics working group ⇨ real-world data in clinical planning♦ Delivered innovative, scalable solutions for business questions/problems ⇨ utilizing appropriate and efficient predictive methods and tools♦ Supported RFPs using predictive methods and simulation ⇨ assessing study execution and program timelines

In June of 2009, I was promoted to the position of Senior Analyst for the Enterprise Transformation Unit, delivering statistical methods support for business transformation initiatives.Key Achievements:♦ Founding Member ⇨ executive working group on EMRs for clinical trial planning♦ Contributing Member ⇨ enterprise business analytics product development strategy♦ As the Senior Analyst ⇨ contributed to the development of department’s first statistical, programming and data support function

Selected to join Quintiles, Inc. in 2005 as a Senior Biostatistician - Global Biostatistics, I served as the Global Lead for a large neurology 6 study program and eCTD submission. In this role, I performed comprehensive clinical study design and analysis, including protocol and statistical analysis plan development. I also led as an adaptive design consultant for the department. Responsibilities & Achievements include:♦ Lead Biostatistician ⇨ 12 Phase III trials (CNS< Oncology, Immunology)♦ Lead Biostatistician ⇨ 5 large Phase IV trials in cardiovascular

ClinForce is a national provider of resource solutions serving the pharmaceutical, biotechnology, medical device and related clinical trials industries.▬▬▬▬▬▬▬▬▬▬▬▬▬In 2004, I joined ClinForce as a Lead Statistician and was responsible for sNDA filing in the CNS therapeutic area. During my tenure in this role, I developed and implemented a new document and specification system for the company.

Rho delivers clinical drug development services including contract research, clinical trial management, regulatory submissions and more.▬▬▬▬▬▬▬▬▬▬▬▬▬As a Biostatistician with Rho, Inc., I delivered statistical consulting and programming support of Phase 2-3 studies and NDA submissions.