Experience

New York Oncology Hematology

• United States
• Hospitals and Health Care
• 100 - 200 Employee

• Manager of Clinical Research Services

  • Jan 2022 - Present

• Supervisor, Research Services

  • Jul 2021 - Jan 2022

• Senior Clinical Research Coordinator

  • Mar 2020 - Jul 2021

  *Screens potential patients for protocol eligibility.*Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol. *Coordinates patient care in compliance with protocol requirements.*May disburse investigational drug and provide patient teaching regarding administration.*Maintains investigational drug accountability. *In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug, and thoroughly documents all findings. *Responsible for accurate and timely data collection, documentation, entry, and reporting.*Schedules and participates in monitoring and auditing activities. *Maintains regulatory documents in accordance with USOR SOP and applicable regulations. *Participates in required training and education programs.*Responsible for education of clinic staff regarding clinical research. *May collaborate with Research Site Leader in the study selection process. *Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors. *Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality. *May be responsible for compiling and reporting protocol activity, accrual data, and research financial information to practice administration and physicians. *May oversee the preparation of orders by physicians to assure that protocol compliance is maintained.*Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting. *Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC.*Maintains strict patient confidentiality according to HIPAA regulations and applicable law


IQVIA
• United States
• Hospitals and Health Care
• 700 & Above Employee
• Clinical Research Associate II

  • Dec 2019 - Mar 2020
• Clinical Research Associate

  • Aug 2018 - Oct 2019
• Clinical Research Coordinator

  • Aug 2015 - Aug 2018

  *Screens potential patients for protocol eligibility.*Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol. *Coordinates patient care in compliance with protocol requirements.*May disburse investigational drug and provide patient teaching regarding administration.*Maintains investigational drug accountability. *In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug, and thoroughly documents all findings. *Responsible for accurate and timely data collection, documentation, entry, and reporting.*Schedules and participates in monitoring and auditing activities. *Maintains regulatory documents in accordance with USOR SOP and applicable regulations. *Participates in required training and education programs.*Responsible for education of clinic staff regarding clinical research. *May collaborate with Research Site Leader in the study selection process. *Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors. *Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality. *May be responsible for compiling and reporting protocol activity, accrual data, and research financial information to practice administration and physicians. *May oversee the preparation of orders by physicians to assure that protocol compliance is maintained.*Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting. *Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC.*Maintains strict patient confidentiality according to HIPAA regulations and applicable law

• Lead Pharmacy Technician

  • Feb 2013 - Aug 2015

• Pharmacy Technician

  • Apr 2005 - Feb 2013