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Corpus Christi Medical Center - Technical Supervisor/Clinical Laboratory Scientist Resume Example

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XXXX, Corpus Christi, Texas 78414
  • Cell: XXX-XXXX-XXX
Clinical Laboratory Scientist with 9 years bench experience and 5 years as a CLIA Federal Regulatory and Compliance Specialist.
  • Blood Banking 
  • Immunology
  • Hematology
  • Coagulation
  • Microbiology
  • Urinanalysis
  • Laboratory quality control
  • Scientific recruitment and educator
  •  42 CDFR 493 Regulatory Affairs and Compliance   Pre analytic, analytic and post analytic laboratory system
  • SOPs
  • ICH
  • GCP
Relevant Experience
  • Generalist Clinical Laboratory Scientist for 9 years with a main focus in blood banking for the last four years . 
  • Regulatory Specialist IV for Texas Department of State Health Services    Conducted complex CLIA (Clinical Laboratory Improvement Amendment) audit surveys in accordance with 42 CFR 493 regulations.
  • Hematopathology Laboratory Manager 
  • Biopharmaceutical Recruiter.  Recruited Regulatory and Clinical staff for positions across the country for the pharmaceutical and biopharmaceutical industry.
Relevant Professional Experience
Corpus Christi Medical Center Corpus Christi, TX Technical Supervisor/Clinical Laboratory Scientist 08/2014 to Current
Perform high complexity laboratory procedures using established and approved protocols in areas such as blood banking, immunology, serology,hematology, chemistry,and microbiology.
Analyze quality control and corrects problems using scientific principles while maintaining accuracy and precision.
Participates in the evaluation of new techniques in the laboratory including method comparison, cost analysis, and establishment of reference intervals; writing and revising technical procedures.
Serve as Clinical Laboratory Science student educator for local universities and colleges.
Texas Department of State Health Services San Antonio, TX CLIA Compliance Specialist IV 06/2008 to 11/2013 Survey Experience: Compiles, reviews and analyzes information from preanalytic, analytic and post analytic processes derived from clinical record reviews of quality control data, quality analysis data, patient charts, consumer and facility staff interviews and on site observations Evaluates management , supervision and quality of care delivery. Determines the validity of allegations in the complaint and compliance with state and federal regulations Plans of Corrections: Evaluates and approves or requests additional information for plans of corrections for deficient practices identified during the survey. Uses state and federal guidelines concerning the necessary elements that constitute an acceptable plan of correction Report Writing: Documents survey findings in written reports. Recommends adverse state enforcement action and federal termination action if applicable Public Relations: Represents the department by making presentations, providing information and testimony , collaborating with customers, other state agencies and federal partners. Provided consultation and pre survey conferences to regulated healthcare facility provides and potential providers to assist them in maintaining compliance with state and federal regulations..
Education and Training
Certification: Clinical Research Associate 2013 Kriger International Research Center, Huntsville, Ontario, Canada
Clinical Trial Monitoring and Research Site Coordination
The International Conference on Harmonization (ICH)
Good Clinical Practice (GCP)
Bachelor of Science: Advanced Clinical Laboratory Science University of Texas Health Science Center San Antonio, San Antonio, TX, USA
Activities and Honors
American Society of Clinical Pathologist Board Certified (ASCP)
National Certified Investigator (NCI) from the Council on Licensure, Enforcement and Regulation Affiliations American Society of Clinical Pathology (ASCP)
Clinical laboratory testing, auditing, consultation, report writing,
presentations, Problem resolution, public relations, quality control, quality assurance, regulatory affairs, staffing, supervision

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