Clinical Research Nurse 3

• May 2022 - Present

Research Nurse Specialist

• Apr 2020 - Present

Quality Assurance Auditor

• Sep 2018 - Apr 2020

Clinical Research Nurse Coordinator

• Oct 2015 - Sep 2018

Registered Nurse, CRC

• Oct 2013 - Oct 2015

Clinical Research Coordinator for late phase dialysis studies. Clinical Research Coordinator for late phase dialysis studies.

Clinical Study Coordinator

• Jun 2013 - Sep 2013

LPN

• Oct 2012 - Jun 2013

skilled nursing bedside carerehabilitation skilled nursing bedside carerehabilitation

Clinical research coordiantor

• Mar 2008 - Jul 2012

- Demonstrates thorough understanding of study medications, dosing procedures, and protocol specifications for all assigned studies while monitoring the safety and wellbeing of study participants at all times. - Serves as point of contact for the participant and Sponsor throughout the clinical study. - Works closely with physicians, Sponsor, and study staff to ensure the protocol is carried out safely and accurately. - Participates in staff training specific to coordination and clinical trial conduct for assigned studies.- Performs the following procedures as assigned: drug accountability and dosing, phlebotomy, EKG, vital signs, admission and discharge, and assessment of Adverse Events.- Has a working knowledge of GCP/ICH guidelines, company SOPs and QA/QC procedures. - Reviews source documents prior to study initiation for accuracy and consistency with the protocol- (continued) Reviews signed laboratory reports, carries out physician orders, and schedules repeat assessments as needed. - Ensures that data including Adverse Events, concomitant medications, and dosing are collected and documented precisely.- Provides clinical care to subjects in the event of a medical emergency including providing BLS/ACLS as needed. - Coordinates the resolution of data discrepancies and queries in a timely manner. - Ensures that all studies are conducted in accordance with Federal, state and protocol requirements, standard operating procedures, and Good Clinical Practice (GCP)- Handles participant complaints efficiently and effectively and ensures that sponsor and participant confidentiality is maintained.

Clinical research Coordinator

• 2012 - 2012

This was a phase I-IV research clinic. Demonstrates thorough understanding of study medications, dosing procedures, and protocol specifications for all assigned studies while monitoring the safety and wellbeing of study participants at all times. - Serves as point of contact for the participant and Sponsor throughout the clinical study. - Works closely with physicians, Sponsor, and study staff to ensure the protocol is carried out safely and accurately. - Participates in staff training specific to coordination and clinical trial conduct for assigned studies. - Performs the following procedures as assigned: drug accountability and dosing, phlebotomy, EKG, vital signs, admission and discharge, and assessment of Adverse Events. - Has a working knowledge of GCP/ICH guidelines, company SOPs and QA/QC procedures. - Reviews source documents prior to study initiation for accuracy and consistency with the protocol - (continued) Reviews signed laboratory reports, carries out physician orders, and schedules repeat assessments as needed. - Ensures that data including Adverse Events, concomitant medications, and dosing are collected and documented precisely. - Provides clinical care to subjects in the event of a medical emergency including providing BLS/ACLS as needed. - Coordinates the resolution of data discrepancies and queries in a timely manner. - Ensures that all studies are conducted in accordance with Federal, state and protocol requirements, standard operating procedures, and Good Clinical Practice (GCP) - Handles participant complaints efficiently and effectively and ensures that sponsor and participant confidentiality is maintained.

The Palace at Kendall Nursing and Rehabilitation Center

• May 2007 - Mar 2008

Skilled nursing Bedside careRehabilitation Skilled nursing Bedside careRehabilitation