Laura Reid is a highly qualified professional, who works in Alexion Pharmaceuticals, Inc main office of which is in 499. on the position of Associate Director, Clinical Quality R and D from 2019. This person has earned professional experience in more than 11 positions at different companies. Laura Reid went to the University of Wisconsin-Madison and got education from 1985 to 2000. This expert has the following professional qualifications: Rac, Regulatory Affairs Certification and Regulatory Affairs Professionals Society (Raps). Raleigh, North Carolina is the city, where this person was known to live. This person's email address and number are easily accessed through SoftwareOfficial on demand.
Name variants:
Laurie Reid,
Lauri Reid,
Lolly Reid
Last updated Jun 02, 2024
Contact Information
Last Update
Feb 1, 2016
Email
l4**@aol.com, la**@premier-research.com
Location
Raleigh, NC
Company
Workplace
Colleagues
Work History
Associate Director, Clinical Quality R and D
121 Seaport Blvd, Boston, MA 02210
from Jul 2019
Senior Auditor, Qa, Risk and Compliance
1 Park Dr SUITE 150, Durham, NC 27709
Organize and lead contracted audits (investigator sites, trial master files, database, study reports etc.) and internal audits (systems, processes, vendors, computer system validation etc.) ...
Jun 1, 2015 — Jun 2018
Associate , Qa and Regulatory Compliance
300 west Morgan St, Durham, NC 27701
Conducted internal project audits and external vendor audits for adherence to clinical trial protocols, company SOPs, and applicable GCP, GLP, CLIA, or GMP regulations and guidelines.
Host...
May 2012 — Aug 2014
Study Director
Supervised team of Study Managers responsible for project management, quality control and data analysis for GLP and GMP studies.
Jun 2010 — Dec 2010
President, Auditor, Scientific and Regulatory Consultant
Wrote SOPs, IND submissions, IDE briefing packages and responses to FDA correspondence. - Audited GCP/GLP and CLIA testing laboratories as well as GLP animal facilities. - Established quali...
Oct 2008 — Apr 2012
Pharmacogenomics Consultant & Technical Writer
Write SOPs and organize quality system to meet CLIA regulations. Prepare proposals and manage pharmacogenetics projects. Supervise the preparation and submission of grants and other fundin...
from Oct 2008
Consultant, Scientific & Regulatory Affairs
Prepared FDA documents in response to pre-IDE submission. Established QSR/GMP program for software used in medical devices. Wrote IRB-approved protocols for software predicting adverse eve...
Jun 2008 — Feb 2009
Senior Director, Genomic Sciences, R&D and Marketing
Sr. Director of Marketing & External Scientific Affairs (2006 to 2007)
Director of Research & Development (2003 to 2006)
Director of Genomic Sciences (2001 to 2003)
Initiated genomic...
Nov 2001 — Dec 2007
Senior Director, Genomic Sciences, R and D and Marketing
4324 south Alston Ave, Durham, NC 27713
Initiated scientific services for Start-up Company using microarray technology. Hired, trained and supervised laboratory personnel. Analyzed data and consulted with Top-10 Pharma Clients. - ...
Nov 2001 — Dec 2007
Director, Genomics Core and Research Assistant Professor
Chapel Hill, NC
Supervised production of microarrays on glass slides using robotic equipment. - Mapped tumor suppressor genes in the imprinted region of human chromosome 11.
Jan 1991 — Oct 2001
Education
1985 — 2000
1985 — 1990
1980 — 1984
Occupations
IT Professional
Software Tester
Technical Writer
Counselor
Scientist
Biotechnology Professional
Computer Specialist
Technical Communicator
Author
Advisor
Biologist
Biological Scientist
Skills
Genotyping
Biomarkers
Microarray
Technical Writing
IVD
Genomics
Biotechnology
Molecular Biology
Lifesciences
Genetics
DNA
PCR
GLP
Biochemistry
DNA sequencing
Fda
Glp
Auditing
Regulatory Affairs
Gcp
Compliance
Quality Assurance
Quality System
Quality Systems Design
Quality System Compliance
Clinical Trials
Sop
Ivd