Jae O.

Jae O. Email and Phone Number

Senior Director of Product Management @ LinkedIn
California, United States
Jae O.'s Location
San Francisco, California, United States, United States
Jae O.'s Contact Details
About Jae O.

With over 15 years of experience in product management, data and analytics, and clinical trials, I am a product leader with expertise in marketing solutions and integrative medicines. As the Director of Product at LinkedIn, I work with an exceptional team that owns Audiences, Insights and Measurement for LinkedIn Marketing Solutions, products that empower customers to reach their audiences, measure their outcomes/ROI, and optimize their marketing/business strategies with LinkedIn. I leverage my skills in management, product development, and AI/ML to deliver innovative and impactful solutions that address the needs and challenges of our customers and partners. I am also a Startup Mentor at First Round Capital, where I share my insights and guidance with aspiring product managers and entrepreneurs. I am passionate about creating products that improve the lives and well-being of people, and I value collaboration, diversity, and social responsibility. I hold a MS in Biophysics and Physiology, Integrative Medicines, and certifications in CSPO and PMP. I am fluent in English, Korean, and French.

Jae O.'s Current Company Details
LinkedIn

Linkedin

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Senior Director of Product Management
California, United States
Website:
linkedin.com
Employees:
23970
Jae O. Work Experience Details
  • Linkedin
    Senior Director Of Product Management
    Linkedin
    California, United States
  • Linkedin
    Director Of Product Management
    Linkedin Sep 2022 - Present
    Sunnyvale, Ca, Us
  • Linkedin
    Group Manager, Product Management - Measurement And Audiences
    Linkedin Jan 2021 - Sep 2022
    Sunnyvale, Ca, Us
    I work with an exceptional team that own Audiences (ad targeting, ABM tools, DMP, AI/ML based audience building, intent prediction, 3rd party integrations), Insights and Measurement (campaign reporting, attribution/conversion tracking, measurement partnerships, data platform) for LinkedIn Marketing Solutions - products that empower customers to reach their audiences, measure their outcomes/ROI, and optimize their marketing/business strategies with LinkedIn.
  • Linkedin
    Principal Product Manager, Audiences
    Linkedin Mar 2020 - Jan 2021
    Sunnyvale, Ca, Us
  • Linkedin
    Senior Product Manager, Audiences
    Linkedin Mar 2018 - Mar 2020
    Sunnyvale, Ca, Us
    Helping businesses grow by empowering them to connect better with their audiences on LinkedIn. Ad targeting, 3rd party data integration, matched audiences/DMP, AI-based audience modeling, ABM products, interests and intent.
  • First Round Capital
    Startup Mentor - Product
    First Round Capital Feb 2021 - Present
    San Francisco, Ca, Us
  • Emissary.Io
    Advisor
    Emissary.Io Jun 2016 - May 2018
    New York, New York, Us
    Advisor on Healthcare and HIPAA-Regulated Data Enterprise SaaS products
  • Google
    Product
    Google Nov 2016 - Feb 2018
    Mountain View, Ca, Us
    (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)
  • Gobalto, Inc.
    Director Of Product - Data & Analytics
    Gobalto, Inc. Sep 2015 - Sep 2016
    (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.
  • Comprehend Systems
    Sr. Product Manager
    Comprehend Systems May 2014 - Aug 2015
    (Health tech)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
  • Comprehend Systems
    Customer Solutions Manager
    Comprehend Systems Nov 2013 - Jun 2014
    • 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
  • Icon Plc
    Clinical Trials Manager
    Icon Plc Mar 2010 - Nov 2013
    Dublin, Ie
    • 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
  • Pharmedout.Org
    Health Policy And Phytomedicines Fellow
    Pharmedout.Org May 2009 - Jul 2009
    • 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.
  • Georgetown University Medical Center
    Clinical Research Fellow, Merenstein Probiotics Lab
    Georgetown University Medical Center Aug 2008 - Jan 2009
    Washington, Dc, Us
    • 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.
  • Pfizer
    Clinical Trials Manager, Ph Ii-Iii (Global)
    Pfizer Aug 2007 - Aug 2008
    New York, New York, Us
    [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
  • African Health Foundation
    Advisory Board
    African Health Foundation Jan 2006 - Mar 2008
    Non-profit organization working to provide education, water, support, and resources to Sub-Saharan African HIV/AIDS communities
  • Cardiovascular Research, Massachusetts General Hospital
    Clinical Researcher, Herman K. Gold Cardiology Research Lab
    Cardiovascular Research, Massachusetts General Hospital Aug 2006 - May 2007
    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
  • Radiology, Massachusetts General Hospital
    Research Assistant, Muscular-Skeletal Radiology
    Radiology, Massachusetts General Hospital Jan 2005 - May 2006
    • 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.
  • Chicano Studies Research Center, Ucla
    Systems Analyst Ii, Web Developer
    Chicano Studies Research Center, Ucla Jan 2001 - Apr 2004
    • 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.

Jae O. Skills

Clinical Trials Clinical Research Clinical Development Product Management Gcp Management Clinical Data Management Pharmaceutical Industry Cro Product Development Biotechnology Business Development Agile Methodologies Risk Analysis Leadership Scrum Saas Project Management Analytics Crm Data Management Fda Clinical Monitoring Data Models Budget Management Client Engagement Ctms Edc Data Analysis Software Documentation Software Development Strategy Software Quality Management Mobile Applications Emr Program Management Research Design Pmp Auditing Business Analysis 21 Cfr Part 11 Outcomes Research Sql R Data Integration Cspo Cross Functional Team Leadership

Jae O. Education Details

  • Georgetown University
    Georgetown University
    Integrative Medicines
  • Harvard University
    Harvard University
    Public Health
  • Ucla
    Ucla
    Developmental Biology / Computer Science

Frequently Asked Questions about Jae O.

What company does Jae O. work for?

Jae O. works for Linkedin

What is Jae O.'s role at the current company?

Jae O.'s current role is Senior Director of Product Management.

What is Jae O.'s email address?

Jae O.'s email address is ja****@****ail.com

What is Jae O.'s direct phone number?

Jae O.'s direct phone number is +131057*****

What schools did Jae O. attend?

Jae O. attended Georgetown University, Harvard University, Ucla.

What are some of Jae O.'s interests?

Jae O. has interest in Harvard University, Pfizer, Los Angeles, University Of California.

What skills is Jae O. known for?

Jae O. has skills like Clinical Trials, Clinical Research, Clinical Development, Product Management, Gcp, Management, Clinical Data Management, Pharmaceutical Industry, Cro, Product Development, Biotechnology, Business Development.

Who are Jae O.'s colleagues?

Jae O.'s colleagues are Johnvsbph0503-234501 Doe, Johnebsib1002-101436 Doe, Kiprono Koech, Johnhzcxf0320-224903 Doe, Video Tester, Muhammad Ishfaq, Alexandrea Hooker.

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