Julia Marshall Graber, MA, CCRP

Julia Marshall Graber, MA, CCRP

Licensed Massage Therapist

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location of Julia Marshall Graber, MA, CCRPMemphis, Tennessee, United States

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  • Timeline

  • About me

    Research Project Coordinator at The University of Tennessee Health Science Center

  • Education

    • The University of Memphis

      2009 - 2011
      Master's Degree Applied Anthropology/Concentration in Medical Anthropology

      Activités et associations :The Society for Applied Anthropology (SfAA)

    • The University of Memphis

      -
      Bachelor's Degree Anthropology magna cum laude
  • Experience

    • Self-Employeed

      Jan 2002 - Sept 2014
      Licensed Massage Therapist

      TN License retired in FEB2020. Trained in Ashiatsu, LaStone, and Swedish modalities.

    • Center for Research on Women (CROW)

      Jan 2009 - Jan 2010
      Graduate Research Assistant

      Assisted with federally funded healthcare Program Evaluation. Program was aimed at reducing infant mortality in Memphis, TN via a lay health advisor model.

    • The University of Memphis

      Jan 2010 - Jan 2011
      Graduate Assistant

      Assisted with Introduction to Cultural Anthropology class

    • Southern Growth Studio

      Sept 2012 - Jan 2013
      Ethnographer/Consumer Research Anthropologist

      Conducted ethnographic data collection, analysis, report writing, and presentations for client projects (while company known as Southern Growth Studio/later rebranded as Epic Pivot).

    • Southern Growth Studio

      Jan 2014 - Sept 2014
      Independent Contractor/Anthropologist
    • Bayer HealthCare Consumer Health via Hill Top Research

      Sept 2014 - Jan 2017
      CRO Study Coordinator

      Worked as Interim Assistant Site Manager as well as Study Coordinator starting in July 2016. Coordinated clinical (product use) and non-clinical (focus group) studies involving OTC medicines and consumer products. Ensured studies were conducted to meet Sponsor's expectations and that all relevant regulations, SOPs, and protocols were followed. Ensured subject safety and data integrity. Managed Study Binders (TMF), created and edited study documents (protocols, consent forms, screeners, case report forms), handled IRB submissions, and assisted with study archival. Also assisted Sponsor with editing Moderator's Reports for non-clinical studies and served as a Non-Physician Investigator or Sub-Investigator on select studies. Voir moins

    • The University of Tennessee Health Science Center

      Jan 2017 - now

      Working in the Department of Preventive Medicine as a Research Project Coordinator on NIH sponsored randomized controlled trials delivering behavioral interventions for weight management and smoking cessation. Managing study team, planning recruitment, executing protocol, physical measurements/data collection, Quality Control, database management, procurement of supplies/medication, monitoring Adverse Events, incentive disbursement, retention strategies, IRB submissions, qualitative data coding, NIH and clinicaltrials.gov reporting, and manuscript editing. Voir moins

      • Research Project Coordinator

        Nov 2017 - now
      • Interventionist

        Jan 2017 - Mar 2019
  • Licenses & Certifications

    • Certified Clinical Research Professional, CCRP

      SOCRA
      Dec 2016