Christine Tran

Experience

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  US Oncology

  Jul 2011 - Oct 2012

  Research Data Coordiantor

  Collect, coordinate, process and control quality of data collected for clinical trials in accordance to protocol information and in compliance with US Oncology Research Standard Operating Procedure. Work with electronic medical records and assist with ensuring patient appointments and assessments occur according to protocol.

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  Texas Medical Center

  Oct 2012 - Apr 2013

  Clinical Research Coordinator

  Conduct research trials in compliance with Good Clinical Practice guidelines, Standard Operating Procedures, and study protocols. Recruit and coordinate subjects through screening, procedure, and follow up. Collect, coordinate and process quality data. Communicate with sponsor throughout trial for regulatory and research trial purposes.

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  Children's National Health System

  Mar 2013 - Oct 2015

  Clinical Research Coordinator

  Conduct research trials in compliance with Good Clinical Practice guidelines, Standard Operating Procedures, and study protocols. Recruit and coordinate subjects through screening, procedure, and follow up. Collect, coordinate and process quality data. Communicate with sponsor throughout trial for regulatory and research trial purposes.Prepare and maintain Institutional Review Board applications, submissions and approvals.

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  Inova Fairfax Hospital

  Aug 2016 - Apr 2017

  Registered Nurse

  Provided compassionate care, life support, and consistent monitoring for critically ill, medically complex and post-surgical pediatric patientsManaged health and recovery of patients according to protocol including, but not limited to, IV administration, medication administration, airway ventilation care, external ventricular drain care and central line access. Collaborated with families and other health care providers on patient care and recovery and modifying plan of care as needed.

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  Weill Cornell Medicine

  Apr 2017 - Nov 2020

  Clinical Research Nurse Specialist

  Reviewed and coordinated lymphoma clinical trials varying from Phase II to Phase I trials that required in depth patient monitoring. Ensure optimal quality of medical care for patients participating in study; Create educational aides and manuals as reference framework for patients and staff as necessary.Participate in continuing education programs including new venous access methods. Educate nursing staff to drug protocols. Assist with updating policies/procedures. Ensure optimal quality of medical care for patients participating in study.Arrange follow-up visits with patient to assess optimal quality of care and applies appropriate physical and psychological assessment to determine any effect of study drug. Implement appropriate intervention in the event of adverse patient response.Assess patient eligibility for inclusion in investigational studies. Review patient history and abstracts and records information; records pre- study lab data; secure baseline laboratory blood work from patient and arrange necessary scans.Review "informed consent" with patient; coordinate and educate patient and medical personnel as to required follow-up tests to be performed; assist physician in preparing IRB documents and maintain correspondence with sponsoring company/agency and IRB.Assure adherence to study requirements according to protocol; monitor study drug according to protocol; monitor and/or perform pharmokinetic studies as detailed in protocol and assist with coordinating laboratory procedures to process, store and ship specimens. Show less

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  Stanford Health Care

  Dec 2020 - Mar 2024

  Provide, coordinate, and facilitate patient care for clinical trial patients in Early Drug Development. This department included Phase I trials for solid tumors and genomic trials. Coordinated with different specialty groups within the Stanford Healthcare system and with local and external oncology offices to ensure optimal patient care and to help improve transition of care. Assisted with standard practice operations. With the help of Patient Education Services, initiated, created and implemented New Patient Letter developed to educated patients about clinical trials and how to better prepare for their visit with links to resources. Show less

  • Assistant Patient Care Manager/Senior Program Manager

    Jan 2022 - Mar 2024

  • Nurse Coordinator

    Dec 2020 - Jan 2022