ASCP-Certified Gynecologic Cytotechnologist

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LISA LEE TRBOVICH, CT (ASCP)

412-***-**** ****.*.********@*****.*** Tampa, FL 33647 www.linkedin.com/in/lisa-trbovich-7976341a2/ CYTOTECHNOLOGIST – GYNECOLOGIC CYTOLOGY

Gynecologic Cytology & Cervical Screening – SurePath & ThinPrep Pap Testing – Microscopic Cytologic Evaluation HPV Testing & Pap/HPV Correlation – Cytology Quality Assurance & QC – CAP/CLIA Regulatory Compliance ASCP-Certified Cytotechnologist and Clinical Laboratory Professional with 25+ years of progressive experience specializing in gynecologic cytology, microscopic specimen evaluation, cytopreparation, and diagnostic quality assurance within high-volume laboratory environments. Expertise spanning SurePath and ThinPrep Pap testing, HPV testing/correlation, limited non- gynecologic cytology, ROSE support, LIS-based specimen management, and cytology QC/rescreen processes, with a strong record of maintaining diagnostic accuracy, specimen integrity, and timely reporting. Proven ability to collaborate closely with pathologists and Molecular Diagnostics teams to support Pap/HPV result correlation, integrated reporting, and efficient turnaround times while maintaining rigorous compliance with CAP, CLIA, quality, safety, and patient data requirements. Holds Clinical Laboratory Supervisor licensure in Florida and CT (ASCP) Cytology certification, complemented by current healthcare laboratory certifications and specialized cytotechnology training. CORE EXPERTISE

Cellular Morphology Analysis Specimen Adequacy Assessment/Verification Cytopreparation & Staining Techniques Non- Gyne Cytology Quality Assurance & Control CAP & CLIA Compliance LIS Documentation PCR Sample Correlation

(Pap/HPV) Diagnostic Accuracy & Error Reduction Initiatives Cross-Functional Collaboration with Pathologists Specimen Identification Chain-of-Custody Integrity Process Optimization & Workflow Efficiency Equipment Troubleshooting & Maintenance Support Cytopathology & Diagnostic Testing Molecular Diagnostics (HPV, PCR) Specimen Processing

(SurePath, ThinPrep) Team Training & Collaboration Patient Data Confidentiality Laboratory Safety Protocols Gynecologic Cytology Screening

LICENSES & CERTIFICATIONS

Clinical Laboratory Supervisor - License Florida Department of Health - Florida SU 58300 08/2028 HIV/AIDS Training for Healthcare Professionals - Certification 08/2026 Preventing Medical Errors: Lab Personnel - Certification 08/2026 Certified Cytotechnologist American Society for Clinical Pathology (ASCP) - PA 129270 PROFESSIONAL EXPERIENCE

07/1998 – 07/2025 • QUEST DIAGNOSTICS • Pittsburgh, PA Tampa, FL Cytotechnologist

Performed microscopic evaluation of gynecologic specimens (SurePath and ThinPrep Pap smears) to ensure precise, efficient, and timely diagnostic interpretations in full compliance with CAP, CLIA, and Quest quality standards. Conducted limited non- gynecologic evaluations, including urine, thyroid, breast, and anal cytology, applying learned ROSE (Rapid On-Site Evaluation) principles to assess specimen adequacy. Utilized Laboratory Information Systems (LIS) for specimen tracking, result entry, and report verification, maintaining full traceability across all stages of analysis. Maintained adherence to quality control, safety, and regulatory protocols, supporting readiness for CAP inspections and internal audits.

Strengthened quality assurance framework by collaborating on updated cytology QC metrics, leading to measurable improvements in specimen adequacy rates.

Participated in interdepartmental collaboration with Molecular Diagnostics to synchronize Pap and HPV result turnaround times (TAT), ensuring integrated and timely patient reporting.

Improved turnaround efficiency by assisting in the cross-functional coordination of Molecular PCR workflows, ensuring concurrent reporting of Pap and HPV results.

LISA LEE TRBOVICH, CT (ASCP) CONTINUED

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Boosted departmental agility through cross-training in SurePath, ThinPrep, and molecular sample preparation, enabling seamless coverage during staffing fluctuations.

Advanced laboratory performance by promoting continuous peer learning and sharing updates on emerging cytotechnology practices and automation trends.

Enhanced diagnostic reliability by integrating precision-based cytologic screening protocols that reduced rescreen discrepancies and unsatisfactory sample rates.

Ensured specimen integrity and identification accuracy through meticulous pre-analytical verification, minimizing reporting errors and improving diagnostic reliability.

Maintained exceptional accuracy rates through disciplined case review, consistent correlation with histopathology, and proactive consultation with pathologists.

Cultivated a culture of accountability and independence, balancing individual diagnostic responsibility with collaborative teamwork to achieve collective laboratory goals.

Supported pathologists in the screening and correlation of abnormal cytologic findings, contributing to accurate and clinically actionable reports.

EDUCATIONAL BACKGROUND

Bachelor of Science (BS) in Biology University of Pittsburgh, Pittsburgh, PA CT (ASCP) - Cytology University of Pittsburgh, Anissa Kanbour School of Cytotechnology, Pittsburgh, PA TECHNICAL PROFICIENCIES

Laboratory Systems & Software: Laboratory Information Systems (LIS) Diagnostic Reporting Systems Quality & Compliance Frameworks: CAP (College of American Pathologists) Standards CLIA (Clinical Laboratory Improvement Amendments) Regulations QA/QC Documentation Systems Patient Data & PHI Compliance Systems Cytology & Diagnostic Techniques: SurePath & ThinPrep Cytology Systems Molecular PCR Sample Processing HPV Testing/Correlation ROSE (Rapid On-Site Evaluation) Support Cytopreparation & Staining Techniques: Microscopic Evaluation Equipment Cytology Quality Control (QC) & Rescreen Audit Tools

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