Denise Stucker

Quality Assurance Analyst, Laboratory Director

Location
grandview, MO (US)
Work Category
QA - Quality Control
Interests
Ways to stay in touch
Email

About Me

I am a highly motivated and focused individual who thrives in a challenging position as well as a dedicated professional with the drive to succeed, as an individual or as part of the team.

Work Experience

  • Jul 2006 - present
    kansas city, MO (US)
    Moderate Complexity Laboratory Director
    LabCorp
    · Responsible for the overall operation and administration of the laboratory, including the employment of competent personnel, ensuring the activities of the laboratory reflect the policies and procedures, State & Federal Laws and all regulatory agencies.
  • Oct 2005 - present
    kansas city, MO (US)
    QA Analyst
    LabCorp
    · Working with Satellite and Stat laboratories in developing, revising and implementing standard operating procedures, QC procedures and policies.
    · Perform quality assurance reviews to ensure that actions taken by program staff are in accordance with applicable regulations, statutes, and/or policies.
    · Lead and participate in monthly meetings and training.


  • Dec 2002 - Oct 2005
    olathe, KS (US)
    Medical Technologist
    Heritage Labs International, LLC
    · Performing patient testing in the serum chemistry department with accuracy and precision.
    · Quality assurance and quality control.
    · Maintenance of all instruments and records.
  • Aug 2000 - Oct 2002
    lenexa, KS (US)
    Clinical Trials Study Coordinator
    Clinical Reference Laboratory
    · Responsible for all portions for study initiation, which includes:
    * Directing all areas of the lab and warehouse for necessary study preparation
    * Writing Laboratory Investigator’s Training Manual and laboratory protocols
    · Perform professional presentations at investigator meetings
    · Responsible for on-going study management which includes:
    * Monitoring sites and identifying any site problems to sponsor
    * On-going training on specimen collection and protocol specifications
    * Participating in conference calls or meetings requested by sponsor
    * Manage pharmokinetic samples for studies
    · Coordinate with the QA/QC officers for correct study specifications
    · Update computer database with all correct study parameters and updates

Education

  • 1994 - 1997
    Bachelor's - Medical Technology & Natural Science
    AVILA UNIVERSITY
    Minors: Chemistry
    Microbiology