Laura Gaines is a qualified expert, working in Icon Plc as a Site Engagement Liaison from 2019. Laura Gaines has earned professional experience in more than 15 positions at various companies. Laura Gaines went to the University of Cincinnati and got education from 2012 to 2016. Cincinnati, Ohio is the city, where this person was known to be living. This person's e-mail and phone can be easily accessed through this website by request.
Name variants:
Laurie Gaines,
Lauri Gaines,
Lolly Gaines
Last updated Jun 02, 2024
Contact Information
Last Update
Sep 9, 2013
Email
la**@cinci.rr.com
Location
Cincinnati, OH
Company
Icon Plc
Workplace
Site Engagement Liaison
Work History
Clinical Enrollment Specialist
650 Dundee Rd SUITE 250, Northbrook, IL 60062
Jun 2016 — Dec 2016
Clinical Research Coordinator Iv and Research Manager
Sep 2013 — Jun 2016
Senior Clinical Research Coordinator
1105 Schrock Rd SUITE 200, Columbus, OH 43229
Nov 2012 — Sep 2013
Clinical Research Coordinator
2600 Clifton Ave, Cincinnati, OH 45202
May 2009 — Dec 2011
Clinical Trial Submissions Coordinator
5375 Medpace Way, Cincinnati, OH 45201
Completed international protocol and amendment submissions to Competent Authorities and Ethics Committees in many countries outside the US
Created and maintained protocol submission status...
May 2006 — May 2009
Research Technician II promoted to Clinical Research Coordinator III
Cincinnati, OH
Mar 2001 — Oct 2003
Project Manager/Medical Writer/Clinical Research Associate
2000 — Jan 2012
Education
2012 — 2016
Occupations
Scientist
Clinical Research Coordinator
Project Manager
Researcher
Survey Researcher
Project Managers
Skills
Neurology
Oncology
Clinical Trials
Gcp
Cro
Ctms
Clinical Monitoring
Clinical Research
Edc
Ich Gcp
Healthcare
Pharmaceutical Industry
Clinical Data Management
Regulatory Submissions
Cro Management
Good Clinical Practice
Clinical Trial Management System
Clinical Development
Research
Project Management
Trial Management
Microsoft Office
Microsoft Excel
Microsoft Word
Medical Devices
Orthopedics
Biobanking
Study Monitoring
Clinical Operations
Clinical Site Monitoring
Drug Development
Electronic Data Capture
Therapeutic Areas
Medidata
Inform
Ind
Regulatory Affairs
Patient Recruitment
Ccra
Genomics
Standard Operating Procedure
Clinical Protocols
Protocol Development
Evidence Based Medicine
Communication
Matrix
Cross Functional Team Leadership
Budgeting