Experience

Meridian Clinical Research

• United States
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Investigational Product Research Coordinator

  • Aug 2021 - Present

  Responsible for identification, administration of, and reconciliation of IP. Initiates and supervises returns/destruction of IP, and associated responsibilities/duties. Demonstrates/maintains correct documentation, and record keeping, Maintenance of un-blinded Binder to ensure the timely inclusion of updated documents therein filed properly within the Binder. Responsible for understanding the correct process flow, clinical administration, and documentation required for un-blinded studies as… Show more Responsible for identification, administration of, and reconciliation of IP. Initiates and supervises returns/destruction of IP, and associated responsibilities/duties. Demonstrates/maintains correct documentation, and record keeping, Maintenance of un-blinded Binder to ensure the timely inclusion of updated documents therein filed properly within the Binder. Responsible for understanding the correct process flow, clinical administration, and documentation required for un-blinded studies as defined by individual protocols as well as the administrations of product. Show less Responsible for identification, administration of, and reconciliation of IP. Initiates and supervises returns/destruction of IP, and associated responsibilities/duties. Demonstrates/maintains correct documentation, and record keeping, Maintenance of un-blinded Binder to ensure the timely inclusion of updated documents therein filed properly within the Binder. Responsible for understanding the correct process flow, clinical administration, and documentation required for un-blinded studies as… Show more Responsible for identification, administration of, and reconciliation of IP. Initiates and supervises returns/destruction of IP, and associated responsibilities/duties. Demonstrates/maintains correct documentation, and record keeping, Maintenance of un-blinded Binder to ensure the timely inclusion of updated documents therein filed properly within the Binder. Responsible for understanding the correct process flow, clinical administration, and documentation required for un-blinded studies as defined by individual protocols as well as the administrations of product. Show less



NEBRASKA, STATE OF

• United States
• 1 - 100 Employee

• Child and Family Services Specialist

  • Aug 2019 - Sep 2021

  Meet with families on a monthly basis, conduct Family Team Meetings, assess families for safety, complete assessments to determine safety and risk, complete assessments that help families determine their strengths and needs, determine the correct community resources to assist families with their needs, make all efforts to ensure the family stays together if possible. Meet with families on a monthly basis, conduct Family Team Meetings, assess families for safety, complete assessments to determine safety and risk, complete assessments that help families determine their strengths and needs, determine the correct community resources to assist families with their needs, make all efforts to ensure the family stays together if possible.



Madonna Rehabilitation Hospitals

• United States
• Hospitals and Health Care
• 500 - 600 Employee

• Phlebotomist

  • Feb 2014 - Jun 2020

  Read and implement doctors' orders and ensure patient safety while collecting blood samples by performing venipuncture or finger stick. Read and implement doctors' orders and ensure patient safety while collecting blood samples by performing venipuncture or finger stick.



Grifols

• Spain
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Quality Associate

  • Feb 2015 - Jul 2015

  Perform daily donor record file review. Perform equipment quality control review. Verification and release of sample shipment. Perform Staging of plasma for shipment. Inspection and release of incoming supplies. Perform weekly employee observations. Assist the Center Quality Manager to ensure that cGMP, SOPs and regulatory requirements are met and followed. Performs a review of the documentation of unsuitable test results and the disposition of the associated units. Documents, investigate, and… Show more Perform daily donor record file review. Perform equipment quality control review. Verification and release of sample shipment. Perform Staging of plasma for shipment. Inspection and release of incoming supplies. Perform weekly employee observations. Assist the Center Quality Manager to ensure that cGMP, SOPs and regulatory requirements are met and followed. Performs a review of the documentation of unsuitable test results and the disposition of the associated units. Documents, investigate, and perform roots cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the products. Perform a review of look back information and waste shipment information. Initiates investigation and reports any supplies that have not met quality specification and requirements prior to use.

• Donor Center Technician

  • Oct 2014 - Jul 2015

  Conducts pre-donation medical screening in accordance with established guidelines, determines Hematocrit and Protein via finger stick. Assesses donor suitability and engages in set-up, monitor and disconnect procedures of the plasmapheresis machine and donors. Provides appropriate feedback to ineligible donor candidates. Promotes customer satisfaction through appropriate interaction and responsiveness to customer needs. Establishes and maintains donor files in an organized and efficient manner,… Show more Conducts pre-donation medical screening in accordance with established guidelines, determines Hematocrit and Protein via finger stick. Assesses donor suitability and engages in set-up, monitor and disconnect procedures of the plasmapheresis machine and donors. Provides appropriate feedback to ineligible donor candidates. Promotes customer satisfaction through appropriate interaction and responsiveness to customer needs. Establishes and maintains donor files in an organized and efficient manner, learns and maintains through familiarity and compliance with all state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvements Amendments (CLIA), and Current Good Manufacture Practice (cGMP).



Celerion

• United States
• Pharmaceutical Manufacturing
• 700 & Above Employee

• Clinical Conduct Specialist

  • Apr 2012 - Nov 2013

  Be proficient in areas such as dosing, blood processing, sample shipping, and CPR. Provide leadership for conduct. Assist Study Managers with study preparation, set up, study meetings; such as initiation meetings and client visits. Administer study specific training. Order supplies for study conduct. Serve as a backup for study conduct as needed.

• Phlebotomist

  • Aug 2010 - Apr 2012

  Drawing blood samples from study participants within time restraints of study protocols. Sample handling and tracking of blood samples. Process and package blood samples.

• Clincial Conduct Officer

  • Aug 2010 - Apr 2012

  Managing and overseeing associates' clock-ins and clock-outs. Managing the clinic and all of the conduct. Ensuring participant and employee safety in case of emergencies.



MDS Pharma Services

• United States
• Pharmaceutical Manufacturing
• 300 - 400 Employee

• Clinical Conduct Associate/Clinical Conduct Technician

  • Sep 2007 - Aug 2010

  • Interpret Specification sheet • Perform vital signs • Assist with blood collection and lab work preparation • Perform ECGs • Handling and processing of urine, feces and saliva. • Retrieve sample inventory • Process blood samples according to specific direction of study protocol • Interpret Specification sheet • Perform vital signs • Assist with blood collection and lab work preparation • Perform ECGs • Handling and processing of urine, feces and saliva. • Retrieve sample inventory • Process blood samples according to specific direction of study protocol