Feb 2021 – Jun 2024 · 3 yrs 4 mos

Nov 2016 – Feb 2018 · 1 yr 3 mos · Mountain View, California

• (Adtech)
• Building smarter search ML-driven ad formats that enrich the user experience on google.com; launched dynamic sitelinks, expanded dynamic ad extensions to i18n markets (structure snippets, callouts, sitelinks)

Jun 2016 – May 2018 · 1 yr 11 mos · San Francisco Bay Area

• Advisor on Healthcare and HIPAA-Regulated Data Enterprise SaaS products

Sep 2015 – Sep 2016 · 1 yr · San Francisco Bay Area

• Context: Joined at <40ppl org size; scaled data-as-a-service offering from 0>1. (2018 acquired by Oracle).
• (Health tech) We built a data-driven, enterprise research SaaS product focused on maximizing value delivered by study start-up teams from site selection to activation through smart workflows and best in class operational analytics.
• Drove evolution of data platform from nightly ETL based data handling to near real-time data processing to support actionable analytics, deep linking applications to/from the analytics product and operation workflow product and the surfacing of a curated data model to support end-business open querying of the integrated dataset for custom reporting.

May 2014 – Aug 2015 · 1 yr 3 mos · Redwood City, CA

• Context: First official Product Manager for the company; joined at company size <12.
• Senior Product Manager, Feb 2015 - Aug 2015
• Managed product development to scale from initial conception and research to development, validation, and analysis in close collaboration with Engineering and Design
• Defined functional requirements and associated metrics (KPIs) to assess product value from delivery to continued development
• Development and associated messaging of overall product roadmap across Sales, Marketing, and Solutions teams; owned project specific roadmaps for UI development and several data pipeline related features
• Defined development of several new feature additions to the core product, including support for data driven workflows, expanded analytical functions for reporting needs, improved in-tool user administration and a single user type optimized analytics UI
• Established Product communications framework to better manage direct customer relationships in order to launch new features to early customers and to involve key clients in the design process
• Supported infrastructure to enable Engineering team transition’s to a formalized Agile development framework
• Extended best practices aligning to Scrum and consistent with Industry-specific regulatory and QA requirements, across the organization to include professional services team and support
• Managed design process to build functionality to improve management of underlying data model with to support the Solutions team
• Negotiated early priority clients' ($18M+ ARR) shift towards a more frequent release schedule as SaaS product despite biotech/pharma industry common practices; including shift to multi-tenancy infrastructure, improved data and product validation procedures
• Conducted continuous competitive analysis and acted as subject matter expert across overall product
• Contributed to internal release validation procedures and best practices in support of new QA staff

Nov 2013 – Jun 2014 · 7 mos · Redwood City, CA

• Project managed as SME (subject matter expert) and first solutions manager for a number of key stakeholder accounts from the company's portfolio as Solutions Manager
• Managed technical delivery of study and datasource integrations
• Worked with lead colleagues to actively review new analytics requirements for custom development
• Progressed real-world applicability of internal dummy-data set in collaboration with lead data architect based on actual clinical development scenarios
• Provided internal guidance regarding industry best practices for analytics relevant to operational metrics, clinical outcomes, risk based management methodology and performance evaluation across various therapeutic areas and design types
• Developed initial assets for customer product education and internal onboarding tools
• Supported customer deployment hands-on from initial adapter setup to customer validation of SaaS instance

Mar 2010 – Nov 2013 · 3 yrs 8 mos · San Francisco Bay Area

• Clinical trials manager and specialized clinical services product manager associated with: statistical analysis, late phase interventional, and phase IIIb-IVa post marketing studies (observational, chart review, registry).
• Project director for several ongoing studies (TAs: oncology, infectious dx, RA).
• Business development activities include bid defense and proposal preparation and attendance, resource management, data/budget projection with emphasis on accurate forecasting, client management, and project cost and timeline modeling.
• Creation and support of study protocols, issue and risk management guidelines, and workflows related to budget management, study & research conduct, data management, and other client project and protocol level processes.
• Study design strategies lead and contributor to the technical, protocol-specific and operational aspects of assigned trials; risk based monitoring and threshold based risk mitigation strategy generation
• Primary coordinator for cross-functional team resourcing and internal/external client relationship management
• Publications focused SAS and Excel dataset review, manuscripts review/editing, and primary publications research in therapeutic areas including, but not limited to neurology, pulmonary, cardiovascular, and medical devices.
• Project operations department contributor for Global PO department, involved in training presentations, operational efficiencies review, business development & management strategies, internal training, and resource management.
• Manage direct reports and mentor junior colleagues
• Therapeutic areas include: neurology, cardiopulmonary (PAH, CF), oncology, rheumatology, infectious diseases

May 2009 – Jul 2009 · 2 mos · Washington D.C. Metro Area

• Contributor in design and implementation of studies focused on evaluating industry funding biases potentially present in continuing medical education (CME) courses and subsequent credits targeted at medical professionals (MD, NP, etc.)
• Drafting papers related to conventional, alternative, and comparative therapies.
• Working with USBG botanists, horticulturalists, and gardeners in plant propagation, classification, hybridization, and identification.
• Phytotherapeutic research and botanical monograph creation; administrating botanical database for medicinal plants garden and creating educational material for medical professionals, students, and researchers.

Aug 2008 – Jan 2009 · 5 mos · Washington D.C. Metro Area

• Subject recruitment and enrollment (screening, informed consent, etc.).
• Monitoring trial subject profiles and data in accordance with protocol follow-up guidelines for adverse events, progress reports, and compliance analysis.
• Managing product supply chain needs based on predicted subject enrollment and budget analysis; arranged delivery of product to sites.
• Public presentations of study design, eligibility requirements, and related data at meetings with groups of potential subjects.
• Interim analysis of study data for statistical and clinical significance in consideration of substantive laboratory data available.

Aug 2007 – Aug 2008 · 1 yr · Greater New York City Area

• [via FSP, Execupharm Inc.]
• Primary contact for all logistical aspects of several global cardiovascular clinical trials according to US FDA, GCP, and ICH regulations in accordance with company SOPs; this includes, but is not limited to regulatory compliance, implementation of technology enabled processes, and complete management of necessary deliverables.
• Creation and support of study protocols, issue management guidelines, investigator meeting materials and workflow related to study conduct, data management, and other center/protocol level processes.
• Responsible for development and maintenance of dynamic study databases (some proprietary to company, others based in excel) related to drug supplies/shipments, subject tracking, and fiscal planning.
• Therapeutic areas included: cardiopulmonary, endocrinology (diabetes, obesity), rheumatology

Aug 2006 – May 2007 · 9 mos · Greater Boston Area

• Initiating and managing several clinical trials related to drug and device related therapies (i.e. drug eluting stents, pre/post-procedural drugs, etc.) for treating coronary artery diseases (CAD), via communication with pharm. and biotech companies, IRB, and other research institutions.
• Conducted statistical and background research on emerging products related to in-house research at both the bench (lab) and clinical levels.
• Maintained extensive databases for clinical data - creating end of term evaluation reports to outline factors and end points related to cost/effectiveness queries, biomarker/clinical result comparisons, and general review.
• Experience in performing small model (live) surgical techniques, including angioplasty and manual vessel dilations. Technical work included, lab bench work (i.e. RNA isolation, cloning, cell culture, etc.) and scientific technology specific work (i.e. network admin., security, wifi integration with proprietary research hardware, etc.)
• Clinicaltrials.gov link: https://clinicaltrials.gov/ct2/show/NCT00476944

Jan 2006 – Mar 2008 · 2 yrs 2 mos · Greater Boston Area

• Non-profit organization working to provide education, water, support, and resources to Sub-Saharan African HIV/AIDS communities

Jan 2005 – May 2006 · 1 yr 4 mos · Greater Boston Area

• Primary engineer for the department’s digitized database of teaching files and related images (based on RSNA MIRC) consolidating data pulled from EMR/EHR and non-digital sources
• Conducted frequent consulting and review sessions with staff and resident physicians on diagnostic cases.
• Assisted in reviews of publications material for textbooks and medical articles for journal publication.

Jan 2001 – Apr 2004 · 3 yrs 3 mos · Greater Los Angeles Area

• Primary administrator for all development/implementation/modification of hardware and software associated with Windows based network and peripherals (blackberries, mobile technologies, etc.); MSW Server administration (Active Directory/MS Exchange)
• Web development consultant and product manager of digital online library for text and archived music (largest Chicano digital music collection as of 2003) overseeing technical implementation and development from wire framing to initial internal site launch.
• Provided end-user support and conducted training seminars for various applications, including Microsoft Office Suite, proprietary software solutions, Mac and MS OS.
• Interdepartmental data security consultant.