Jason C. Cole, Phd

Jason C. Cole, Phd Email and Phone Number

President and Principal Scientist @ Los Angeles, CA, US
Los Angeles, CA, US
Jason C. Cole, Phd's Location
Los Angeles Metropolitan Area, United States, United States
Jason C. Cole, Phd's Contact Details

Jason C. Cole, Phd personal email

n/a

Jason C. Cole, Phd phone numbers

About Jason C. Cole, Phd

My career is a synergy of advanced people skills with advanced technical skills. With people, I work to elicit diverse and articulate input, build consensus, and share information on complex issues in a comprehensible manner for international stakeholders and audiences. From a technical side, my goal is to bring the most rigorous, accurate, and widely received methods available in a manner that makes them accessible to all parties involved.Specialties: Management of, and collaboration with, internal and external experts in the persuit of collaborative goals. I am an expert on building and maintaing international relationships, business development, staff management and development, workshops and presentations.Patient reported outcomes development, use/selection, interpretation, and dossiers; all psychometrics and statistical analysis; HEOR planning and study execution.

Jason C. Cole, Phd's Current Company Details
P3 Research

P3 Research

President and Principal Scientist
Los Angeles, CA, US
Jason C. Cole, Phd Work Experience Details
  • P3 Research
    President And Principal Scientist
    P3 Research
    Los Angeles, Ca, Us
  • P3 Research Consulting
    President & Principal Scientist
    P3 Research Consulting Apr 2021 - Present
    We provide industry leading partnership to develop strategy for Patient Reported/Centered Outcomes, Clinical Outcomes Assessments, and the communication strategies around these for small to large sized pharmaceutical/biotechnology companies seeking to bring the voice of the patient as a central theme for marketed and in-development products.
  • Zs Associates
    Managing Principal/Partner
    Zs Associates Oct 2016 - Apr 2021
    Evanston, Il, Us
    As a next step to expand ZS Associates' Market Access and Pricing solutions, I was brought in to start and lead a Global Health Economics and Outcomes Research practice. These services are managed through our 20+ offices around the world.
  • Ppd
    Executive Director & Lead: Global Health Economics & Outcomes Research
    Ppd Sep 2014 - Oct 2016
    Wilmington, Nc, Us
    As part of the Real World Outcomes, GHEOR efforts at PPD are applied to support a panoply of services throughout the development and post approval lifecycle of pharmaceutical, biotech, and medical device therapies. One of my core assignments was to grow the GHEOR team through a variety of techniques. Along with key hires, we also developed a strategic alliance with HealthCore to expand our offerings and available data resources, and we acquired Evidera to massively expand our in-house GHEOR, RWO, and Epidemiological services. I served as a key executive in all of these expansion efforts. As GHEOR evolved at PPD, I brought about the integration of GHEOR with the rest of company by overseeing the development of key SOPs, leading committees focused on methods and innovation, and aiding the P2-P3 and late-state research teams with critical BD and study team support.
  • Covance
    Senior Director & Lead: Patient Reported Outcomes Group
    Covance Dec 2013 - Sep 2014
    Princeton, New Jersey, Us
    The Covance PRO Group was part of the Market Access division, Global Health Economics & Outcomes Research group. I led a rapidly expanding and international group of PRO experts in charge of advancing Covance's breadth and depth of patient ported outcomes (PROs) consulting repertoire. All three PRO specialty areas reported to me: PRO Clinical Trial Strategy & Execution, PRO Development & Validation, and ePRO Consulting. In concert with the leadership of GHEOR, I directed the development of the vision, strategy, and tactical execution for PRO strategies around the globe for our group. In this manner, I am also in charge of directing the BD efforts for the group and helping to ensure our Prospective Studies group and the PRO group interact with other Covance divisions (e.g., Clinical Development Services) to ensure BD and project support are provided. I also served as an internal and regulatory expert on PRO matters, as projects dictated.
  • Covance
    Director, Lead: Patient Reported Outcomes Group
    Covance Nov 2009 - Dec 2013
    Princeton, New Jersey, Us
    As part of the Covance’s Market Access (CMA) group, I was in charge of advancing Covance's breadth and depth of patient reported outcomes (PROs) consulting repertoire. I provided KOL-level input on psychometrics, advanced statistics, power analyses, PRO dossiers, and other PRO-related consulting. In addition to overseeing many of the PRO-related projects, I was also an integral part of the business-development team striving to expand relationships with current Covance clients and establish new relationships for CMA. As part of business development, I communicated CMA’s unique capabilities and services, drew attention to our signature client service, and developed proposals with integrated consulting throughout CMA’s health economic and outcomes research offerings as well as the rest of our CRO.
  • Marshall Goldsmith School Of Management
    Adjunct Professor
    Marshall Goldsmith School Of Management Aug 2007 - Dec 2009
    San Diego, Ca, Us
    I taught Advanced Statistics II for doctoral students enrolled in the industrial/organizational psychology program at MGSM. The class covered factor analysis (EFA, CFA), advanced regression, logistic and loglinear analyses, missing data techniques, and power analysis.
  • Amgen
    Denosumab Oncology, Global Health Economics
    Amgen Dec 2008 - 2009
    Thousand Oaks, Ca, Us
    I was responsible for multiple aspects of value evidence generation in support of denosumab’s value propositions in the oncology indications, focusing on patient reported outcomes, health utilities, retrospective database analyses, and observational research. The phase 3 and 4 goals I oversaw primarily involved the delay of bone metastasis, including overseeing development of the global value dossier, development of disease specific utilities, meta-analysis of various data sources, development of the cost-effectiveness and budget-impact model, and overall planning for the direction of this indication.I also served as an internal expert on all matters of patient-reported outcomes, longitudinal modeling, power analysis, and missing data issues, including to various internal review boards, biostats, a special R&D-wide group on translation services reform, and throughout the GHE department.
  • Consulting Measurement Group
    President & Senior Research Scientist
    Consulting Measurement Group Jun 1999 - Dec 2008
    As a senior research scientist, I have been primarily involved in planning/overseeing outcomes projects. I have been the lead scientist on: dozens of development and validation projects for outcomes measures; several complex economic modeling projects (cost-effectiveness, price elasticity, and larger macroeconomic models); scores of analysis and publication/dissemination of outcomes data; consulting on regulatory issues related to dossiers and SAPs; and much more. As president, I oversee all issues related to team building, forecasting and tracking of economic of institutional goals, reporting to our board of directors, development and adherence of SOPs, and more.
  • Qualitymetric Incorporated
    Director & Senior Scientist
    Qualitymetric Incorporated Aug 2004 - Sep 2008
    Johnston, Rhode Island, Us
    I was the director of business development (BD) for, and senior scientist in, QualityMetric’s External Science division. As a director of BD, I acted as a scientific liaison in this role, helping clients understand the array of services available to them given their project needs and timelines. I also provided scientific review of strengths and weaknesses for various project approaches in light of their particular needs. Finally, I oversaw the proposal development and ensure it captures the client’s needs accurately with a budget and timeline that were appropriate for all parties.As a senior scientist, I conducted and supervised team personnel in the design and implementation of statistical, methodological, and scientific plans for client research in health outcomes. Studies I oversaw include FDA Phase 2-4 clinical trials (and related international regulatory agencies), including power analyses, study design, analysis planning, label claim planning and dossiers, PRO development and validation, and clinical trial analyses. My expertise was used in all health outcomes, including use and development of PROs, the complete label claims pursuit process from initial planning to dossier submission and postmarketing activities, planning and interpreting economic modeling, and navigating through the various differences between international governmental regulatory agencies. I also oversaw various statistical techniques (both designing SAPs and conducting/interpreting results), including variants of structural equation modeling, advanced missing data handling, item response theory, various forms of longitudinal analyses, nonparametric analyses, and logistic and parametric regression. My duties also included much writing for peer-reviewed publication and presentation. Additionally, I was in charge of in-house training for statistics and measurement at QualityMetric’s consulting division.
  • Ucla Cousins Center For Psychoneuroimmunology
    Senior Statistician
    Ucla Cousins Center For Psychoneuroimmunology Jul 2002 - Aug 2004
    Los Angeles, Ca, Us
    As a Senior Statistician for the Cousins Center for Psychoneuroimmunology, my responsibilities were both research-oriented and supervisory (Center Director: Michael Irwin, MD). Along with the supervision of statistics personnel, I designed and implemented statistical plans for grant-funded research in PNI including latent growth curve modeling, standard and multigroup structural modeling, item response theory, and various forms of repeated measures analyses. My duties also included providing statistical consultation for investigators throughout our center and affiliated groups as well as much writing for academic publication

Jason C. Cole, Phd Skills

Outcomes Research Clinical Trials Health Economics Clinical Research Statistics Clinical Study Design Patient Reported Outcomes Research Strategy Pharmaceutical Industry Data Analysis Patient Outcomes Market Access Cross Functional Team Leadership Research Design Oncology Management Biotechnology Regulatory Submissions Meta Analysis Edc Cro Health Outcomes Global Health Health Economics And Outcoms Research Outcomes Biostatistics Analysis Epidemiology Drug Development Heor Clinical Development Health Policy International Research Leadership Global Strategy Life Sciences Fda Healthcare Pharmaceutics

Jason C. Cole, Phd Education Details

  • Alliant International University-San Diego Campus
    Alliant International University-San Diego Campus
    Clinical Psychology
  • Alliant International University-San Diego Campus
    Alliant International University-San Diego Campus
    Clinical Psychology
  • Uc Irvine
    Uc Irvine
    Psychology

Frequently Asked Questions about Jason C. Cole, Phd

What company does Jason C. Cole, Phd work for?

Jason C. Cole, Phd works for P3 Research

What is Jason C. Cole, Phd's role at the current company?

Jason C. Cole, Phd's current role is President and Principal Scientist.

What is Jason C. Cole, Phd's email address?

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What is Jason C. Cole, Phd's direct phone number?

Jason C. Cole, Phd's direct phone number is (855) 972*****

What schools did Jason C. Cole, Phd attend?

Jason C. Cole, Phd attended Alliant International University-San Diego Campus, Alliant International University-San Diego Campus, Uc Irvine.

What are some of Jason C. Cole, Phd's interests?

Jason C. Cole, Phd has interest in Children, Environment, Education, Human Rights, Arts And Culture, Health.

What skills is Jason C. Cole, Phd known for?

Jason C. Cole, Phd has skills like Outcomes Research, Clinical Trials, Health Economics, Clinical Research, Statistics, Clinical Study Design, Patient Reported Outcomes, Research, Strategy, Pharmaceutical Industry, Data Analysis, Patient Outcomes.

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