Experience

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

• United States
• Research Services
• 200 - 300 Employee

• Repository Program Specialist

  • Jan 2023 - Present

  United States



The Henry M. Jackson Foundation for the Advancement of Military Medicine

• United States
• Research Services
• 700 & Above Employee

• Clinical Research Coordinator- Contractor

  • Jul 2016 - Feb 2023

  Rockville, MD Manages regulatory issues for all protocols upon receipt of IRB approval Maintains accurate, regulatory-compliant program/study binders Coordinates the donation process with potential donors and medical examiners to obtain documentation of informed consent from legally authorized representatives for tissue donations Coordinates efforts of all agencies involved in the protocol approval process; develop and maintain relationships with collaborating investigators and institutions Works… Show more Manages regulatory issues for all protocols upon receipt of IRB approval Maintains accurate, regulatory-compliant program/study binders Coordinates the donation process with potential donors and medical examiners to obtain documentation of informed consent from legally authorized representatives for tissue donations Coordinates efforts of all agencies involved in the protocol approval process; develop and maintain relationships with collaborating investigators and institutions Works closely with scientific and technical staff to support the implementation of regulatory processes within the laboratory and repository functions Works closely with the PI to seek appropriate approvals for all communication and outreach including providing assistance with the development of website and strategic communications plan for the repository Show less



The Henry M. Jackson Foundation for the Advancement of Military Medicine

• United States
• Research Services
• 700 & Above Employee

• Health Specialist- Contractor

  • Jan 2016 - Mar 2016

  Rockville, MD Provide project oversight for the OPCRO OD in order to maximize the effective use of resources within OPCRO Track information within the DAIDS Enterprise System (DAIDS-ES) to ensure that it is kept current and accessible to OPCRO staff Manage information on the OPCRO “Community Page” on the DAIDS Portal, other assigned Community pages, and assigned sub-Portal pages Participate on DAIDS working groups and committees to… Show more Provide project oversight for the OPCRO OD in order to maximize the effective use of resources within OPCRO Track information within the DAIDS Enterprise System (DAIDS-ES) to ensure that it is kept current and accessible to OPCRO staff Manage information on the OPCRO “Community Page” on the DAIDS Portal, other assigned Community pages, and assigned sub-Portal pages Participate on DAIDS working groups and committees to communicate information to OPCRO staff Work with the OPCRO Director and OPCRO’s servicing Administrative Officer to track OPCRO OD’s research management and support (RMS) budget Provide guidance in developing and implementing standardized internal OPCRO administrative policies and procedures, financial/budgetary reports, and maintenance of specialized report Updated Statement of Work (SOW), and managed deliverables and timelines Show less



Social & Scientific Systems

• Research Study Coordinator- Contractor

  • Mar 2015 - Jan 2016

  Bethesda, Maryland Supervised research assistants and data entry personnel Performed data management and data clean-up of active research studies Constructing database for sample tracking Performs quality control functions for content and accuracy of data Match and complete enrollment processes for control subjects Prepares research and regulatory documents and coordinates NIH IRB annual and interim submissions Completes study registration and eligibility criteria, obtains medical records… Show more Supervised research assistants and data entry personnel Performed data management and data clean-up of active research studies Constructing database for sample tracking Performs quality control functions for content and accuracy of data Match and complete enrollment processes for control subjects Prepares research and regulatory documents and coordinates NIH IRB annual and interim submissions Completes study registration and eligibility criteria, obtains medical records Conducts bi-weekly team meetings, monthly coordinator meeting and completes all administrative reports for enrollment tracking Show less



Mary Washington Healthcare

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Polysomnographer Technician/ Charge Tech

  • Apr 2011 - Mar 2015

  Fredericksburg, Virginia Prepare, calibrate, and determine proper functioning of equipment required for testing procedures. Perform appropriate physiologic calibrations for proper signals. Apply all sensors and electrodes according to standard guidelines and regulations. Document all clinical events and score all sleep staging and respiratory in compliance with AASM guidelines. Perform data management and scanning all patient information into patients chart for MD review. Cross trained in EEG lab and all administrative… Show more Prepare, calibrate, and determine proper functioning of equipment required for testing procedures. Perform appropriate physiologic calibrations for proper signals. Apply all sensors and electrodes according to standard guidelines and regulations. Document all clinical events and score all sleep staging and respiratory in compliance with AASM guidelines. Perform data management and scanning all patient information into patients chart for MD review. Cross trained in EEG lab and all administrative tasks for the Sleep disorders Center department. Show less



Eastern Virginia Medical School

• United States
• Higher Education
• 700 & Above Employee

• Clinical Research Assistant

  • Feb 2009 - May 2010

  Norfolk, Virginia I was the acting coordinator on Investigator Initiated Trials. I created all source documents, spreadsheets and databases per protocol. Performed all recruitment, screening, and enrollment of all study subjects per exclusion and inclusion criteria. Performed all required testing per protocol ( vitals, neurological assessments, labwork). I collected, entered and analyzed all data and prepared and presented abstracts and presentations of results. Performed Quantitative Sensory Testing and Cardiac… Show more I was the acting coordinator on Investigator Initiated Trials. I created all source documents, spreadsheets and databases per protocol. Performed all recruitment, screening, and enrollment of all study subjects per exclusion and inclusion criteria. Performed all required testing per protocol ( vitals, neurological assessments, labwork). I collected, entered and analyzed all data and prepared and presented abstracts and presentations of results. Performed Quantitative Sensory Testing and Cardiac Autonomic Nervous System testing. Show less



Gastroenterology Associates of Tidewater, PLLC

• Clinical Research Assistant/Front desk Receptionist

  • Sep 2008 - Feb 2009

  Chesapeake, Virginia Checked in patients for clinic office appointments, handled all patient consults and medical histories. Input research data for monitors using EMR programs. Also assisted with protocol visits for research patients.



Michigan Institute for Clinical and Health Research

• Medical Assistant/Externship

  • Apr 2008 - Jun 2008

  University of Michigan I was performing a medical assistant externship in a clinical research department. I collected and processed data per work protocols, updated protocol books, set up labs and testing supplies per visit and protocol. I attended all Initiation meetings and Research Development Core Meetings



United States Army National Guard

• Unit Supply Sergeant

  • Feb 2000 - May 2008

  Maintained accountability of equipment valued in excess of 800,000 dollar's. Developed and implemented Standard Operating Procedures using attention to detail. Provided combat support and trained soldiers in certain army customs



Kriger Research Group International

• Biotechnology
• 1 - 100 Employee

• Clinical Research Associate/Research Project

  • Oct 2006 - Dec 2006

  This position was a final project in completing the professional development program at Kriger. I prepared Case Report Form's, managed study timelines and randomization lists. Developed and implemented site initiation, and routine monitoring and closing checklists. Designed and set up logs, tracking systems, and gathered post marketing survey information. Also coordinated investigators meetings.