Billie Thomas, CCRP
Clinical Research Coordinator at Vivent Health- Claim this Profile
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Bio
Credentials
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Certified Clinical Research Coordinator
ACRPMay, 2011- Nov, 2024 -
IATA Certification
IPAKJan, 2008- Nov, 2024
Experience
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Vivent Health
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United States
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Hospitals and Health Care
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100 - 200 Employee
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Clinical Research Coordinator
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Oct 2020 - Present
Works with Phase II-IV HIV industry-sponsored and investigator-initiated clinical trials in meeting study specific goals and timelines, preparing for and following study protocols, and monitoring visits. Strong role model, well-organized, multi-tasked and detail-oriented individual with an exemplary attitude and behavior who demonstrates flexibility and an exceptional level of customer service. Recruits and coordinates research subjects. Possesses an understanding of clinical trial protocols, FDA regulations, and ICH/GCP Guidelines. Show less
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Cerner Corporation
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United States
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IT Services and IT Consulting
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700 & Above Employee
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Independent Contractor
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2017 - Present
To collect information about the demographic characteristics, symptoms, OIs, treatments, and laboratory values of a dynamic cohort of ambulatory HIV positive patients. The main object is to assess the efficacy, durability, and adverse effects of antiretroviral therapy and clinical practice. To collect information about the demographic characteristics, symptoms, OIs, treatments, and laboratory values of a dynamic cohort of ambulatory HIV positive patients. The main object is to assess the efficacy, durability, and adverse effects of antiretroviral therapy and clinical practice.
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APEX Research
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Germany
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Clinical Research Coordinator
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2015 - 2020
Daily management of concurrent HIV clinical trials including all regulatory and institutional documents for human subject research. Patient interaction included. Informed consent, lab draws, vitals, EKGs, and data collection. Coordinated and responded to all requests for data in case report information from the sponsor/CRO. Daily management of concurrent HIV clinical trials including all regulatory and institutional documents for human subject research. Patient interaction included. Informed consent, lab draws, vitals, EKGs, and data collection. Coordinated and responded to all requests for data in case report information from the sponsor/CRO.
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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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Research Coordinator II
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2014 - Mar 2015
Ensures IRB approved protocols are implemented and followed. Executes formal consent process and monitors patient status and safety; collects and organizes research data; schedules and conducts study specific training and site in-services to study related staff on new or amended protocols; educates patients the their families about treatment and possible side effects. Assists with new staff mentoring and training. Duties typically include a larger study load with more complex or high enrolling trials. Show less
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Denver Health
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United States
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Hospitals and Health Care
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700 & Above Employee
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Researcher I
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2012 - 2013
Responsible to implement and coordinate a portfolio of research studies conducted through the MICU. Types of current studies include sepsis, acute lung injury, severe alcohol withdrawal syndrome, neurological dysfunction and acute respiratory distress syndrome. Duties include specimen processing and running, data collection and management, and education to MICU team during patient enrollment while adhering to regulatory compliance Responsible to implement and coordinate a portfolio of research studies conducted through the MICU. Types of current studies include sepsis, acute lung injury, severe alcohol withdrawal syndrome, neurological dysfunction and acute respiratory distress syndrome. Duties include specimen processing and running, data collection and management, and education to MICU team during patient enrollment while adhering to regulatory compliance
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Denver Infectious Disease Consultants
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Greater Denver Area
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Research Coordinator
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2005 - 2012
Patient Care: Pre-screens, interviews, and recruits participants for upcoming studies. Practices active listening, provides patient education, and answers the questions / concerns of clinical subjects. Makes participants feel comfortable and maintains a relaxed atmosphere. Documentation/ Administration: Processes consent forms, source documents, and case report forms for test subjects. Updates and processes enrollment forms, protocol amendments, 1572s and CVs. Administers electronic clinical research forms and regulatory documents for the Institutional Review Board. Reviews participant questionnaires and participates in investigator meetings. Distributes investigational drug and provide patient teaching regarding administration. Maintain IP accountability. In collaboration with physician, review patients for change in condition, AE’s, concomitant medical use, protocol compliance, response to study drug and thoroughly document all findings. In collaboration with physician, review patients for change in condition, AE’s, concomitant medical use, protocol compliance, response to study drug and thoroughly document all findings. Show less
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Rocky Mountain Cancer Center
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Greater Denver Area
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Medical Assistant
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2000 - 2007
Administration: Created monthly reports to analyze lab productivity. Managed the order and stocking of all lab supplies. Coordinated and followed up on daily laboratory-related procedures and communications. Helped implement practice's quality assurance and control program. Ensured compliance with HIPAA, CLIA and OSHA regulations while improving patient care/satisfaction. Laboratory Work: Demonstrated proficiency in taking patient medical histories and vital signs, as well as in performing venipunctures, injections and various diagnostic procedures and ancillary tests such as urinalysis, bone marrow biopsies and EKGs. Show less
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Education
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Rockford Career College
Associate of Science - AS, Applied Science