Vicky Brunk

Clinical Affairs Consultant

Vicky Brunk has been working as a Vice President Clinical Affairs at Trireme Medical, Llc since 2018. Furthermore, the professional has professional experience at more than 11 companies using similar skills. Vicky has a total work experience of 14+ years. Vicky attended school at the The George Washington University School of Medicine and Health Sciences from 2006 to 2009. This expert received the following certifications: Regulatory Affairs Professionals Society (Raps), Association of Clinical Research Professionals, and Rac. Vicky Brunk is proficient in English. York, Pennsylvania is the place where Vicky presently lives. You can search for Vicky Brunk's phone number and email. We can also provide you exhaustive contact information upon request.
Name variants:
Victoria Brunk

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Contact Information

Last Update
Jul 11, 2022
Email
vb**@comcast.net
Location
York, PA

Workplace

TriReme Medical, LLC
Vice President Clinical Affairs

Pleasanton, CA

Industry

Medical Devices, Mfg Surgical/Medical Instruments, Surgical and Medical Instruments

Work History

Vice President Clinical Affairs

7060 Koll Center Pkwy SUITE 300, Pleasanton, CA 94566
Jul 2018 — Apr 2019

Vice President of Clinical Affairs

Apr 2015 — Jun 2018

Clinical Affairs Consultant

Providing clinical consulting services for the medical device industry.
from Aug 2010

Director, Clinical Affairs

Mar 2010 — Aug 2010

Director, Clinical Affairs

May 2007 — Mar 2010

Senior Manager

Jan 2007 — Apr 2007

Clinical Research Manager of Field Operations

710 Medtronic Pkwy, Minneapolis, MN 55432
Oct 2004 — Jan 2007

Senior Clinical Research Associate

Illinois
Mar 2004 — Oct 2004

Clinical Research Specialist

Mar 2003 — Mar 2004

Clinical Research Associate

Nov 2000 — Mar 2003

Clinical Research Coordinator

2838 Leaf Shade Dr SUITE B, Ellicott City, MD 21042
Apr 2000 — Oct 2000

Occupations

Counselor
Executive
Vice President
Advisor
Chief Executive

Skills

Clinical Trials
Clinical Research
Medical Devices
Clinical Development
Cro
Cardiology
Clinical Study Design
Fda
Interventional Cardiology
Sop
Therapeutic Areas
Regulatory Affairs
Diabetes
Clinical Monitoring
Iso 13485
Protocol
Ich Gcp
Pharmaceutical Industry
Ctms
Pma
Neurology
Gcp
Cross Functional Team Leadership
Edc
Clinical Data Management
Regulatory Submissions
Clinical Operations
U.s. Food and Drug Administration
Cro Management
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