Bridget Gonzales

Sr. Director, Educational Programs at Association of Clinical Research Professionals
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Contact Information
us****@****om
(386) 825-5501
Location
United States, US

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Molly Downhour

Bridget was a project manager for the oncology phase I program at HonorHealth. Bridget is solution oriented and easily developed positive relationships with the sponsors and CROs. She improved our clinical trial budgets and contracts resulting in a significant increase in revenue. She was also instrumental in implementing our CTMS system. I relied heavily on her insights and experience in the industry.

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Credentials

  • CRQM
    Quality Management Institute
    Jan, 2019
    - Nov, 2024
  • CCRC
    Association of Clinical Research Professionals
    Sep, 2009
    - Nov, 2024

Experience

  • ACRP - Association of Clinical Research Professionals
    • United States
    • Industry Associations
    • 1 - 100 Employee
    • Sr. Director, Educational Programs
      • Mar 2018 - Present

      Working closely with a wonderful group of volunteers to help develop training programs in order to grow dynamic clinical research professionals in our ever changing industry. Using a tool box of tools I have acquired along my 13 plus years of experience in the clinical research industry and being the resource that I wish I had as a Director/Manager. Working closely with a wonderful group of volunteers to help develop training programs in order to grow dynamic clinical research professionals in our ever changing industry. Using a tool box of tools I have acquired along my 13 plus years of experience in the clinical research industry and being the resource that I wish I had as a Director/Manager.

  • Medix™
    • United States
    • Staffing and Recruiting
    • 700 & Above Employee
    • Subject Matter Expert, Clinical Research
      • Mar 2016 - Mar 2018

      Responsible for business development and consulting operations. Working with organizations such as research sites, CROs and Sponsors to strategize and implement cost saving solutions for growing clinical research teams by focusing on quality talent and site operations. Responsible for business development and consulting operations. Working with organizations such as research sites, CROs and Sponsors to strategize and implement cost saving solutions for growing clinical research teams by focusing on quality talent and site operations.

  • ACRP - Association of Clinical Research Professionals
    • United States
    • Industry Associations
    • 1 - 100 Employee
    • Chapter President, North Texas ACRP Chapter
      • 2017 - 2018

  • HonorHealth
    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Manager, Research Business Operations
      • Aug 2015 - Feb 2016

    • Clinical Project Manager
      • Mar 2014 - Aug 2015

  • Clinical Trials of Arizona
    • Glendale, AZ
    • Site Director
      • Aug 2011 - Nov 2013

      Oversight of all aspects of the clinical research site including the study feasibility process, contract/budget negotiations, clinical trial activities, management of Investigator relationships and staff training and maintenance of training. Oversight of all aspects of the clinical research site including the study feasibility process, contract/budget negotiations, clinical trial activities, management of Investigator relationships and staff training and maintenance of training.

  • Clinical Trials of Texas, A Flourish Research Site
    • United States
    • Research Services
    • 1 - 100 Employee
    • Quality Assurance/Quality Control Manager
      • 2008 - 2011

      • Assisted in creating, maintaining and revising the site Standard Operating Procedures (SOP) • Oversaw the source creation process for all studies to ensure compliance with the protocol, SOPs as well as GCPs.• Performed chart reviews of selected studies to ensure compliance and accuracy• Implemented a QC/Data Entry process and department

    • Clinical Research Coordinator
      • 2007 - 2008

      • Conducted all assigned clinical research protocols in accordance with the protocol, site SOPs and FDA guidelines• Recruitment of patients into assigned protocols• Source document creation, completion and data entry into assigned eCRFs• Phlebotomy, administration of vital signs, ECG, ABIs and IM and Subcutaneous injections

  • Accelerated Enrollment Solutions
    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Clinical Research Coordinator
      • Jul 2005 - Aug 2007

      • Conducted all assigned clinical research protocols in accordance with the protocol, site SOPs and FDA guidelines • Source document creation, completion and data entry into assigned eCRFs • Phlebotomy, administration of vital signs, ECG, ABIs and IM and Subcutaneous injections • Conducted all assigned clinical research protocols in accordance with the protocol, site SOPs and FDA guidelines • Source document creation, completion and data entry into assigned eCRFs • Phlebotomy, administration of vital signs, ECG, ABIs and IM and Subcutaneous injections

  • U.S. Air Force Reserve
    • United States
    • Armed Forces
    • 700 & Above Employee
    • Medical Service Apprentice
      • 1997 - 2001

Education

  • Capella University
    Master of Education - MEd, Training and Performance Improvement
    2019 - 2021
  • CSU Sacramento
    Bachelor of Science (B.S.), B.S. Health Sciences/Community Health Education

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