Lisa Majchrowicz Preston is a high-level professional, working in Prosciento, Inc main office of which is in 300. on the position of Associate Director of Cra Services since 2018. Lisa Majchrowicz Preston has earned professional experience in more than 22 positions at different companies. Lisa Majchrowicz Preston went to the The State University Of New Jersey and got education there from 2008. Murrieta, California is the area, where this professional was known to live. This professional's contacts are accessed through SoftwareOfficial by request.
Name variants:
Alice Preston,
Elisa Preston,
Elizabeth Preston,
Melissa Preston
Last updated Jun 03, 2024
Contact Information
Last Update
Jul 11, 2022
Email
pr**@allergan.com, li**@quintiles.com, si**@hotmail.com
Location
Murrieta, CA
Company
Prosciento, Inc.
Workplace
Associate Director of Cra Services
Work History
Associate Director of Cra Services
855 3Rd Ave SUITE 3340, Chula Vista, CA 91911
from Nov 2018
Senior Clinical Research Associate
1 Baxter Pkwy, Deerfield, IL 60015
Clinical Study Team Lead for Global Phase 3 Hemophilia Study
Lead Cross Functional Team meetings
Vendor Management
Vendor and site budget/contract negotiations and payment processing
Ma...
Sep 2009 — Dec 2011
Cra Manager and Lead Cra
50 Technology Dr, Irvine, CA 92618
Recruit, hire and train CRA study personnel
Develop training materials
Conduct CRA study specific and SOP training
Review and Approve timesheets, monitoring reports and expense reports
...
Jul 2008 — Aug 2009
Senior Cra
Initiated and generated source documents, ICFs, monitoring tools, enrollment logs, drug accountability logs, and various other study materials needed for a successful trial
Reviewed protoc...
2007 — 2008
Clinical Research Site Manager
Trained and mentored new CRA personnel
Lead CRA for multi-center, international Oncology study
Developed territory by identifying qualified
investigators
Met 100% of all study deadlines...
2005 — 2007
Regional Cra
2200 Renaissance Blvd SUITE 400, King Of Prussia, PA 19406
Mentored new CRA personnel
Reviewed Monitoring Visit Reports for fellow CRAs
Performed quality control review of data collected at trial sites to ensure compliance with study protocols, F...
2005 — 2006
Regional Cra
Trained/mentored Jr. CRA personnel
Reviewed Monitoring Visit Reports for fellow CRAs
Supported site investigators and their staff to ensure adherence to Good Clinical Practice, FDA regula...
2004 — 2005
Cra
Managed a Phase III, international, multicenter oncology study
Prepared multicenter EC, REB and IRB submission documentations.
Assisted management in territory development by identifying ...
2001 — 2004
Regulatory Affairs Specialist
Supervised Return Center personnel
Conducted internal audits
Assisted in preparing 510k submissions to the FDA for device approval
Maintained and updated device listing files, facility r...
1999 — 2001
Education
2008 — 2008
2004 — 2004
2000 — 2001
Certificate in Science of Regulatory Affairs for the Drug and Biologic Industry
San Diego, CA
from 2000
Occupations
Executive
Deputy Director
Manager
Deputy Manager
Chief Executive
Operations Manager
Skills
Clinical Trials
Clinical Research
Gcp
Healthcare
Regulatory Submissions
Good Clinical Practice
Pharmaceutical Industry
Clinical Operations
Resourcing
Planning Budgeting and Forecasting
Clinical Development
Clinical Research Experience
Budgeting
Global Clinical Operations
Team Leadership
Strategic Planning
Creative Problem Solving