Stephen Polach Email & Phone Number | 2018-Present: Study Coordinator: “Prospective, Multi-Site, Method Comparison Clinical Study of the ResistancePlus MG Diagnostic Accuracy in Detecting M. genitalium and Mutations Associated with Azithromycin Resistance”, Industry Funded, SpeeDx Pty. Ltd. Principal Investigator: Clair Kaplan, APRN. 2017-Present: Study Coordinator: “Clinical Utility Study to Evaluate: Clinical performance of cobas HPV for use on the cobas 6800/8800 Systems using cervical samples collected in PreservCyt for identification of high-grade cervical disease; and Clinical performance of CINtec PLUS Cytology on the VENTANA BenchMark ULTRA instrument for identification of high-grade cervical disease when used as a reflex test in high-risk HPV-positive women; cX8-HPV-435/D032425, Industry Funded, Roche Ventana. Principal Investigator: Clair Kaplan, APRN. 2015-Present: Study Coordinator: Performance of the cobas HPV Test Using Samples Collected in SurePath Preservative Fluid for Identification of High-Grade Cervical Disease When Used as an Adjunct to Cervical Cytology in Women ≥30 Years and as a Primary Screening Test in Women ≥25 Years/COB-HPV-301. Industry Funded: Roche Molecular Systems. Principal Investigator: Timothy Spurrell, MD.

Stephen Polach

2018-Present: Study Coordinator: “Prospective, Multi-Site, Method Comparison Clinical Study of the R...
509 Plantation StreetApartment 215, Worcester, United States

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Stephen Polach’s Email stephen.polach@ppfa.org

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Stephen Polach’s Location 509 Plantation StreetApartment 215, Worcester, United States

Stephen Polach’s Current Industry Planned Parenthood Of Southern New England

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Work Experience

Planned Parenthood Of Southern New England

Advanced Clinic Assistant - Telehealth Assistant - Virtual Services Assistant - Medical Assistant

2012-05-01 00:00:00 - Present

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Stephen Polach is located at
509 Plantation StreetApartment 215, Worcester, United States

Stephen Polach is a 2018-Present: Study Coordinator: “Prospective, Multi-Site, Method Comparison Clinical Study of the ResistancePlus MG Diagnostic Accuracy in Detecting M. genitalium and Mutations Associated with Azithromycin Resistance”, Industry Funded, SpeeDx Pty. Ltd. Principal Investigator: Clair Kaplan, APRN. 2017-Present: Study Coordinator: “Clinical Utility Study to Evaluate: Clinical performance of cobas HPV for use on the cobas 6800/8800 Systems using cervical samples collected in PreservCyt for identification of high-grade cervical disease; and Clinical performance of CINtec PLUS Cytology on the VENTANA BenchMark ULTRA instrument for identification of high-grade cervical disease when used as a reflex test in high-risk HPV-positive women; cX8-HPV-435/D032425, Industry Funded, Roche Ventana. Principal Investigator: Clair Kaplan, APRN. 2015-Present: Study Coordinator: Performance of the cobas HPV Test Using Samples Collected in SurePath Preservative Fluid for Identification of High-Grade Cervical Disease When Used as an Adjunct to Cervical Cytology in Women ≥30 Years and as a Primary Screening Test in Women ≥25 Years/COB-HPV-301. Industry Funded: Roche Molecular Systems. Principal Investigator: Timothy Spurrell, MD.