Charles Freeman

Co-Founder and CPO at SiteAI
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Contact Information
us****@****om
(386) 825-5501
Location
San Antonio, US

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Experience

    • United States
    • Software Development
    • 1 - 100 Employee
    • Co-Founder and CPO
      • May 2022 - Present

      San Antonio, Texas, United States Given my Founder and Clinical Trial industry experience with Element Research Group, I have been leading the SiteAI solution development especially from feature and usability perspectives. I am the first end user in mind when we develop our modules that are designed to accelerate Clinical Trials.

    • United States
    • Research Services
    • 1 - 100 Employee
    • CEO
      • May 2015 - Present

      San Antonio, Texas Area Founder and CEO of Element Research Group whose mission is to revolutionize clinical trials one study at a time. With 7 years and 150+ trials in the experience column, we are going strong with our sophisticated data approach for obtaining clinical trials, trial implementation and patient success. We take pride in meeting and exceeding our enrollment goals and only participate in studies where we can deliver the committed/estimated number of patients while exceeding clinical trial… Show more Founder and CEO of Element Research Group whose mission is to revolutionize clinical trials one study at a time. With 7 years and 150+ trials in the experience column, we are going strong with our sophisticated data approach for obtaining clinical trials, trial implementation and patient success. We take pride in meeting and exceeding our enrollment goals and only participate in studies where we can deliver the committed/estimated number of patients while exceeding clinical trial quality standards. Show less

    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Chief Operating Officer
      • Jan 2014 - Apr 2015

      Boerne, TX Oversee all operations of clinical research Review budgets and coordinate with CEO for approval Develop tracking strategies for research trials, budgets and other aspects of clinical research to improve flow Oversee property management and tenants for JMF Ventures (same owners for TTS Research) Responsible for hiring new employees Oversee Human Resources Responsible for all CFO duties including company budgets, profit/loss comparison, budget implementation Coordinate with… Show more Oversee all operations of clinical research Review budgets and coordinate with CEO for approval Develop tracking strategies for research trials, budgets and other aspects of clinical research to improve flow Oversee property management and tenants for JMF Ventures (same owners for TTS Research) Responsible for hiring new employees Oversee Human Resources Responsible for all CFO duties including company budgets, profit/loss comparison, budget implementation Coordinate with marketing companies for study success

    • Business Manager
      • Feb 2013 - Dec 2013

      Boerne, TX Develop polices and procedures for study implementation, retention and successful completion Hire, interview and train new employees Coordinate and supervise all clinical trials Oversee regulatory Create charts, graphs to track clinical trials success Review Clinical Research Associates reports for each trial

    • Regulatory Affairs
      • Apr 2009 - Feb 2013

      Boerne, TX Develop and implement strategies for regulatory submission and approvals Manage regulatory teams and provide guidance Review and change ongoing projects as needed Negotiate with outside agencies as needed to resolve key regulatory issues Prepare responses to inquires from regulatory authorities. Hire, train, and supervise regulatory staff. Coordinate and prepare document packages for regulatory submissions ensuring compliance with FDA Prepare outlines, summaries, status… Show more Develop and implement strategies for regulatory submission and approvals Manage regulatory teams and provide guidance Review and change ongoing projects as needed Negotiate with outside agencies as needed to resolve key regulatory issues Prepare responses to inquires from regulatory authorities. Hire, train, and supervise regulatory staff. Coordinate and prepare document packages for regulatory submissions ensuring compliance with FDA Prepare outlines, summaries, status reports, graphs, charts, tables and slides for distribution and communication to other departments. Coordinate with institutional review boards for regulatory changes, submission and questions

    • Clinical Research Coordinator
      • May 2007 - Apr 2009

      Boerne, TX Coordinated 20 clinical trials (Allergy, Asthma, COPD, Diabetes, Hypertension and Pediatric) Successful patient retention and study goals. Improve patient flow and documentation Trained new coordinators Work with PI's Introduced patient recruitment strategies Patient scheduling Lab procedures

Education

  • Texas A&M University
    Bachelor of Science (B.S.), Biology, General
    2010 - 2012
  • Northwest Vista College
    Associate's degree Science, Biology/Biological Sciences, General

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