Angelia M Riley

Manager, Simmons Comprehensive Cancer Center Clinical Research Office Regulatory Operations

Angelia M Riley is a eficient professional, that works in Ut Southwestern Medical Center main office of which is in 104. on the position of Manager, Simmons Comprehensive Cancer Center Clinical Research Office Regulatory Operations from 2020. Angelia gained professional experience in more than six positions at various companies. Angelia M Riley went to the Tui University and got education there from 2006 to 2008. Fort Worth, Texas is the area, where the professional was lastly known to be settled. Angelia M Riley's phone and email are easily accessed through SoftwareOfficial by request.
Name variants:
Angelia Riley
Last updated Jul 02, 2024

Contact Information

Last Update
Jul 11, 2022
Email
mi**@yahoo.com, an**@childrens.com
Location
Fort Worth, TX

Workplace

UT Southwestern Medical Center
Manager, Simmons Comprehensive Cancer Center Clinical Research Office Regulatory Operations

Industry

Hospital & Health Care

Work History

Manager, Simmons Comprehensive Cancer Center Clinical Research Office Regulatory Operations

5323 Harry Hines Blvd, Dallas, TX 75390
from Feb 2020

Manager, Clinical Research

2016 — Dec 9, 2016

Team Lead

1935 Medical District Dr, Dallas, TX 75235
Jan 1, 2015 — Jan 1, 2016

Qa Associate

2626 Cole Ave SUITE 825, Dallas, TX 75204
2010 — 2012

Clinical Research Coordinator

1935 Medical District Dr, Dallas, TX 75235
2007 — 2010

Regulatory and Compliance Officer

6020 west Parker Rd SUITE 200, Plano, TX 75093
Jan 1, 2004 — Jan 1, 2007

Education

2006 — 2008
1997 — 2001

Occupations

Executive
Manager
Operations Manager

Skills

Regulatory Affairs
Clinical Trials
Quality Assurance
Gcp
Compliance
Quality Systems
Auditing
Clinical Research
Microsoft Office
Fda
Problem Solving
Medical Devices
Process Improvement
Oncology
Glp
Capa
Sop
Iso 13485
Pharmaceuticals
Team Building
Mentoring
Gmp
Healthcare
Clinical Study Design
Study Coordination
Training
Research Design
Sop Development
Adverse Event Reporting
Study Startup
Regulations
Cro
Clinical Development
Irb
Immunology
Infectious Diseases
Ctms
Protocol
Edc
Regulatory Submissions
Clinical Data Management
Ich Gcp
Regulatory Requirements
Pharmaceutical Industry
Institutional Review Board
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