Alice Marie Lorenzo

Na Director Regulatory Affairs-- Remote

Alice Marie Lorenzo is a skilled expert, who works in ACR Image Metrix main office of which is in 3310. on the position of Director, Quality Assurance and Regulatory Compliance from 2012. This person has earned professional experience in more than five positions at various companies. Alice Marie Lorenzo went to the Widener School of Law and received education there from 2012 to 2014. This professional has the following professional qualifications: Regulatory Affairs Certification and Regulatory Analysis and Compliance. Collegeville, Pennsylvania is the area, where this professional was known to be living. This expert's email address and number can be easily accessed through this website by request.
Name variants:
Alicia Lorenzo, Alyce Lorenzo, Alisa Lorenzo, Alissa Lorenzo, Alyssa Lorenzo, Allie Lorenzo, Ally Lorenzo, Ali Lorenzo, Elsie Lorenzo, Lisa Lorenzo
Last updated Jun 28, 2024

Contact Information

Last Update
Jul 14, 2022
Email
al**@comcast.net
Location
Collegeville, PA
Company
ACR Image Metrix

Workplace

Director, Quality Assurance and Regulatory Compliance

Work History

Director, Quality Assurance and Regulatory Compliance

Philadelphia, PA
ACR Image Metrix is a CRO specializing in providing imaging services to the pharmaceutical, device and biotechnology industries. As a part of the American College of Radiology, ACR Image Met...
from Nov 2012

Administrative Director Office of IND-IDE Support

IND/IDE Support Office, Office of Clinical and Translational Research
Jun 2009 — Nov 2012

Administrative Director, Clinical Trials

Mar 2008 — Jun 2009

Senior Associate, Regulatory Affairs

2007 — 2008

Clinical Quality Auditor

2000 — 2001

Occupations

Executive
Director
IT Professional
Software Tester
Chief Revenue Officer
Scientist
Biotechnology Professional
Chief Administrative Officer
Operations Manager
Computer Specialist
Chief Executive
Biologist
Biological Scientist

Skills

Clinical Trials
Clinical Research
Regulatory Affairs
Gcp
Fda
Pharmaceutical Industry
Regulatory Submissions
Quality Assurance
Sop
Biotechnology
21 Cfr Part 11
Cro
Clinical Development
Ctms
Life Sciences
Cro Management
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