Experience

Hammond-Henry Hospital

• Hospitals and Health Care
• 1 - 100 Employee

• Quality and Safety Coordinator

  • Aug 2023 - Present



University of Iowa

• United States
• Hospitals and Health Care
• 1 - 100 Employee

• Clinical Trials Research Associate

  • Mar 2023 - Aug 2023

  Functions as a member of the Clinical Trials Research team to plan, deliver, and evaluate the health care provided to research protocol patients. Creates, populates, maintains, and enhances multiple databases containing clinical and research information obtained through review of patient charts and samples, lab reports and other related information and in a manner that complies with Institutional Review Board requirements and in response to physician and research needs and… Show more Functions as a member of the Clinical Trials Research team to plan, deliver, and evaluate the health care provided to research protocol patients. Creates, populates, maintains, and enhances multiple databases containing clinical and research information obtained through review of patient charts and samples, lab reports and other related information and in a manner that complies with Institutional Review Board requirements and in response to physician and research needs and requirements. Assists in the design, development, execution and administration of data entry for protocols and clinical studies. Follows study participants; manages collection of data including maintaining records of patient visits/interviews. Enters protocol patient data on electronic databases ensuring that all prerequisites have been completed and are within the required parameters. Monitors compliance, gathers and maintains data, creates worksheets, treatment flow sheets and assorted tools to provide source documentation of protocol treatment procedures; triages telephone calls from patients and families to facilitate clinic visits for medical care/emergent care needs; assists in obtaining prescription medications; provides follow-up for treatment related complications. Serves as liaison to local physicians/hospitals to facilitate care of protocol patients when hospitalized at outside institutions; provides notification to the Principal Investigator, Study Sponsor, and FDA as required per protocol. Assists in maintaining documentation of protocols and relevant data, follow-up correspondence, and summaries. Assists in the preparation of materials for reports to be written by faculty and staff on various oncology protocols and in compiling summary data for inclusion in various reports used for analysis and submission to study sponsors. Show less Functions as a member of the Clinical Trials Research team to plan, deliver, and evaluate the health care provided to research protocol patients. Creates, populates, maintains, and enhances multiple databases containing clinical and research information obtained through review of patient charts and samples, lab reports and other related information and in a manner that complies with Institutional Review Board requirements and in response to physician and research needs and… Show more Functions as a member of the Clinical Trials Research team to plan, deliver, and evaluate the health care provided to research protocol patients. Creates, populates, maintains, and enhances multiple databases containing clinical and research information obtained through review of patient charts and samples, lab reports and other related information and in a manner that complies with Institutional Review Board requirements and in response to physician and research needs and requirements. Assists in the design, development, execution and administration of data entry for protocols and clinical studies. Follows study participants; manages collection of data including maintaining records of patient visits/interviews. Enters protocol patient data on electronic databases ensuring that all prerequisites have been completed and are within the required parameters. Monitors compliance, gathers and maintains data, creates worksheets, treatment flow sheets and assorted tools to provide source documentation of protocol treatment procedures; triages telephone calls from patients and families to facilitate clinic visits for medical care/emergent care needs; assists in obtaining prescription medications; provides follow-up for treatment related complications. Serves as liaison to local physicians/hospitals to facilitate care of protocol patients when hospitalized at outside institutions; provides notification to the Principal Investigator, Study Sponsor, and FDA as required per protocol. Assists in maintaining documentation of protocols and relevant data, follow-up correspondence, and summaries. Assists in the preparation of materials for reports to be written by faculty and staff on various oncology protocols and in compiling summary data for inclusion in various reports used for analysis and submission to study sponsors. Show less



Hammond-Henry Hospital

• Hospitals and Health Care
• 1 - 100 Employee

• Emergency Preparedness & Safety Coordinator

  • May 2022 - Mar 2023

• Safety Specialist

  • Apr 2020 - May 2022

• Certified Personal Trainer

  • Oct 2017 - Apr 2020

• Service Specialist

  • Aug 2016 - Aug 2018



Geneseo High School

• 1 - 100 Employee

• Assistant Softball Coach

  • Feb 2018 - Mar 2023



Southern Illinois University School of Medicine

• United States
• Higher Education
• 200 - 300 Employee

• Graduate Research Assistant

  • Aug 2014 - Aug 2016

  Studied reproductive immunology. Specifically focused on endometriosis, looking for possible links/markers to the immune system and microbiome. Studied reproductive immunology. Specifically focused on endometriosis, looking for possible links/markers to the immune system and microbiome.



University of Illinois Urbana-Champaign

• United States
• Higher Education
• 700 & Above Employee

• Undergraduate Research Assistant

  • Oct 2013 - May 2014