Yolanda Gordon

Travel Clinical Research Coordinator at Care Access
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Contact Information
us****@****om
(386) 825-5501
Location
Dallas, Texas, United States, US

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Experience

    • United States
    • Research Services
    • 400 - 500 Employee
    • Travel Clinical Research Coordinator
      • Sep 2022 - Present

    • United States
    • Research Services
    • 700 & Above Employee
    • Country Approval Specialist
      • Sep 2021 - Present

    • United States
    • Non-profit Organizations
    • 1 - 100 Employee
    • Certified Nursing Assistant
      • May 2016 - Sep 2021

      -Feed, bathe and dress patients -Take patients vital signs -Serve meals, make beds and keep rooms clean -Setup medical equipment and assist with some medical procedures -Answer calls for help and observe changes in a patient’s condition or behavior -Feed, bathe and dress patients -Take patients vital signs -Serve meals, make beds and keep rooms clean -Setup medical equipment and assist with some medical procedures -Answer calls for help and observe changes in a patient’s condition or behavior

    • United States
    • Hospitals and Health Care
    • 1 - 100 Employee
    • Clinical Research Coordinator
      • Nov 2020 - Aug 2021

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Clinical Research Recruitment Specialist
      • Mar 2019 - Jul 2019

      -Receive incoming and outgoing calls for subjects interested in clinical trial -Screen clinical study volunteers -Maintain a database of clinical study volunteers -Assist with sales, marketing, and outreach efforts as needed -Maintain and improve study documents and volunteer records such as consent forms -Interview prospective study subjects -Receive incoming and outgoing calls for subjects interested in clinical trial -Screen clinical study volunteers -Maintain a database of clinical study volunteers -Assist with sales, marketing, and outreach efforts as needed -Maintain and improve study documents and volunteer records such as consent forms -Interview prospective study subjects

    • United States
    • Medical Practices
    • 1 - 100 Employee
    • Clinical Research Coordinator
      • Aug 2018 - Feb 2019

      -Coordinate Clinical trials in accordance with the sponsor’s protocol, site SOPS, FDA Code of Federal Regulations and good clinical practices -Recruit and screen potential subjects for clinical trials -Obtain informed consent for subjects -Conduct subjects study visits according to protocol -Assist with ISS & TMF document -Coordinate Clinical trials in accordance with the sponsor’s protocol, site SOPS, FDA Code of Federal Regulations and good clinical practices -Recruit and screen potential subjects for clinical trials -Obtain informed consent for subjects -Conduct subjects study visits according to protocol -Assist with ISS & TMF document

  • Presbyterian Village North
    • Dallas/Fort Worth Area
    • Certified Nursing Assistant
      • Sep 2017 - Feb 2018

      -Feed, bathe and dress patients -Take patients vital signs -Serve meals, make beds and keep rooms clean -Setup medical equipment and assist with some medical procedures -Answer calls for help and observe changes in a patient’s condition or behavior -Feed, bathe and dress patients -Take patients vital signs -Serve meals, make beds and keep rooms clean -Setup medical equipment and assist with some medical procedures -Answer calls for help and observe changes in a patient’s condition or behavior

    • United States
    • Medical Practices
    • 1 - 100 Employee
    • Clinical Research Coordinator
      • Aug 2015 - Aug 2017

      -Coordinate clinical trials in accordance with the sponsor’s protocol, site SOPs, FDA Code of Federal Regulations and Good Clinical practices. -Recruit and screen potential subjects for clinical trials. -Obtain informed consent for subjects and conduct visits with subjects -Coordinate clinical trials in accordance with the sponsor’s protocol, site SOPs, FDA Code of Federal Regulations and Good Clinical practices. -Recruit and screen potential subjects for clinical trials. -Obtain informed consent for subjects and conduct visits with subjects

    • United States
    • Medical Practices
    • 1 - 100 Employee
    • Patient Recruiter / Researcher Coordinator
      • Sep 2010 - Aug 2015

      -Conducts telephone interviews with potential study patient using study questionnaire in order to determine eligibility -Recruits and makes selection decisions regarding potential study participants -Manages the patient database -Handles incoming and outgoing calls pertaining to patient recruiting and scheduling -Makes cold calls using the Community Research database -Maintains patient tracking for all current studies via the database -Research and contact venues for health fairs and community outreach (Health Care Clinics, etc.) -Coordinate clinical trials in accordance with the sponsor’s protocol, site SOPs, FDA Code of Federal Regulations and Good Clinical practices. -Recruit and screen potential subjects for clinical trials. -Obtain informed consent for subjects. -Conduct subject study visits according to protocol. Show less

    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Traveling Clinical Research Coordinatorf
      • Feb 2011 - Feb 2012

      -Go to various subjects home to draw blood for clinical trials. -Report AE’s -Take vital signs -Shipping and processing of blood -Reporting to CRC of any problems with the subjects -Go to various subjects home to draw blood for clinical trials. -Report AE’s -Take vital signs -Shipping and processing of blood -Reporting to CRC of any problems with the subjects

    • United States
    • Research Services
    • 700 & Above Employee
    • Research Assistant
      • Mar 2004 - Sep 2010

      -Taking v/s according to protocol. -Monitoring meal according to protocol. -Practicing GCP’s reading and following protocol according to study -Taking v/s according to protocol. -Monitoring meal according to protocol. -Practicing GCP’s reading and following protocol according to study

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