Min Bartoe

Min Bartoe: Email & Phone Number

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Senior Health Authority Reporting Clinician at Johnson & Johnson|United States

Position:

Senior Health Authority Reporting Clinician at Johnson & Johnson

Location:

United States

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Last updated: 2025-09-27
Updated: 2025-09-27

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Work Experience 34 years

Senior Health Authority Reporting Clinician at Johnson & Johnson

Apr 2018 - Current

Subject Matter Expert in Medical Device Reporting/Auditing at QualityHub

Nov 2014 - Apr 2018

Senior Clinical Consultant at Validant

Aug 2013 - Apr 2018

Quality Assurance (QA) Clinician at Oxford Global Resources

Dec 2015 - May 2016

Medical Device Recall Specialist/Protocol Analyst at MAETRICS

Jun 2013 - Aug 2013

Product Safety Expert consultant at IS International Services, LLC

Sep 2012 - May 2013

US Drug Safety Operation Officer at UCB

Mar 2011 - Sep 2012

Drug Safety Operations Manager at IQVIA

Dec 2010 - Mar 2011

Drug Safety and Risk Management Senior Associate II at Biogen

Nov 2006 - Oct 2010

Expert Clinical Drug Safety Manager at ImClone Systems, a wholly-owned subsidiary of Eli Lilly and Company

May 2006 - Aug 2006

Drug Safety Scientist/team lead at Novartis

Apr 2005 - Apr 2006

Consultant in Regulatory Safety at PFIZER PHARMACEUTICALS (K-force Agency)

May 2004 - Apr 2005

Site Support to Senior Medical Director in Drug Surveillance at Baxter International Inc.

Jan 2004 - Apr 2004

Medical Documentation Reviewer at Prudential Financial

Jan 2000 - Jan 2003

Call Center Manager for Aetna/Consulting for 1 year project at Coram CVS/specialty infusion services

Jan 1999 - Nov 1999

Home Health Aids Supervisor and Primary Nurse/Medical Surgical and Hospice at patient care almost family

May 1995 - Sep 1998

Post surgical/Trauma/medical surgical nurse-supervisory to License Practical Nurses and Assistants at UMDNJ

Jun 1993 - May 1995

Nursing Assistant/Nursing Student at UMDNJ

Jan 1992 - Jan 1994

Min Bartoe started working in 1992, then the employee has changed 16 companies and 17 jobs. On average, Min Bartoe works for one company for 2 years 1 month.

Their professional focus is Biotechnology, Cardiology, and Clinical Development across 3 core areas.

Education

BSN at Rutgers University–Newark

high school diploma at Cedar Ridge High School

Walden University

Skills

Vendor Management, Neurology, Oncology, Software Documentation, Cross-functional Team Leadership, Standard Operating Procedure (SOP), Clinical Trial Management System (CTMS), CTMS, Medical Devices, CRO Management, Regulatory Submissions, Life Sciences, Pharmacovigilance, Drug Development, Infectious Diseases, Clinical Trials, U.S. Food and Drug Administration (FDA), Good Clinical Practice (GCP), Compliance Management, Quality Assurance, Clinical Research, Training, Biotechnology, Pharmaceutics, Sop, Healthcare, Cardiology, Regulatory Affairs, Pharmaceutical Industry, Medical Affairs, ICH-GCP, Clinical Development, GCP, Corrective and Preventive Action (CAPA), CRO, FDA

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