Yolanda Gordon
Travel Clinical Research Coordinator at Care Access- Claim this Profile
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Bio
Experience
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Care Access
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United States
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Research Services
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400 - 500 Employee
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Travel Clinical Research Coordinator
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Sep 2022 - Present
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PPD
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United States
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Research Services
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700 & Above Employee
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Country Approval Specialist
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Sep 2021 - Present
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AIDS Services of Dallas
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United States
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Non-profit Organizations
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1 - 100 Employee
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Certified Nursing Assistant
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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
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Urology Clinics of North Texas, PLLC
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United States
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Hospitals and Health Care
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1 - 100 Employee
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Clinical Research Coordinator
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Nov 2020 - Aug 2021
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Accelerated Enrollment Solutions
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United States
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Pharmaceutical Manufacturing
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700 & Above Employee
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Clinical Research Recruitment Specialist
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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
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Sanova Dermatology
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United States
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Medical Practices
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1 - 100 Employee
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Clinical Research Coordinator
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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
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Presbyterian Village North
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Dallas/Fort Worth Area
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Certified Nursing Assistant
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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
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MENTER DERMATOLOGY RESEARCH INSTITUTE, LLC
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United States
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Medical Practices
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1 - 100 Employee
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Clinical Research Coordinator
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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
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Allergy Immunology Clinic
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United States
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Medical Practices
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1 - 100 Employee
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Patient Recruiter / Researcher Coordinator
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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
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ClinForce
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United States
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Traveling Clinical Research Coordinatorf
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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
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Covance
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United States
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Research Services
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700 & Above Employee
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Research Assistant
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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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