Leslie Wells

Senior Clinical Research

Leslie Wells is a qualified expert, who works in Covance main office of which is in 969. on the position of Senior Clinical Research Associate since 2011. This expert gained professional experience in more than nine positions at different companies. Leslie Wells went to the Vanderbilt School of Nursing and got education from 2000 to 2003. Little Rock, Arkansas is the city, where this professional was known to live. Leslie Wells's email address and phone number can be easily accessed through SoftwareOfficial by request.
Name variants:
Lesley Wells, Les Wells
Last updated Jun 03, 2024

Contact Information

Last Update
Jul 9, 2022
Email
lj**@aol.com
Location
Little Rock, AR
Company

Workplace

Covance
Senior Clinical Research Associate

Industry

Pharmaceuticals

Work History

Senior Clinical Research Associate

206 Carnegie Ctr Dr, Princeton, NJ
Currently contracting consultant responsible for conducting site selection, initiation and interim monitoring visits ensured study sites conducted all clinical trial activities, including ...
from Sep 2011

Senior Clinical Research Associate

Provided total site management; site qualification visits, completed study start up/initiation, interim and close out visits. Created study start up SIV training slides, study drug dosing ...
Aug 2009 — Aug 2011

Independent Drug Monitor

Responsible for ensuring clinical sites adhere to FDA/ICH/GCP requirements/guidelines, as well as the sponsor protocol for study drug storage, reconstitution, study drug accountability, whil...
Nov 2008 — Jul 2009

Regional Cra

14506a University Point Pl, Tampa, FL 33613
Conducted site monitoring visits for an ophthalmology device clinical trial provide required monitoring documentation, i.e. site confirmation letters, monitoring reports and follow-up lett...
Mar 2009 — Jun 2009

Senior Clinical Research Associate

May 2007 — Oct 2008

Clinical Research Associate

Durham, NC
Conducted interim monitoring visits with total site management; utilized InForm EDC electronic Case Report Forms (eCRFs) for monitoring data entry/queries.
Jul 2006 — Jun 2007

Clinical Research Associate

Conducted site qualification visits, SIV and Routine Monitoring Visits with total site management for Phase II trial utilizing RxTrials EDC electronic Case Report Forms (eCRFs) for monitorin...
Jul 2005 — Jul 2006

Clinical Research Associate

14506a University Point Pl, Tampa, FL 33613
Vascular Closure Device studying improvement in hemostasis time: Review protocol and amendments for development of source documents and paper Case Report Forms; Provide interim monitoring vi...
Jan 2006 — Jun 2006

Clinical Research Associate

As a permanent employee received CRA training with therapeutic and protocol specific training for inpatient renal transplant clinical trial to provide interim monitoring visits with total si...
Jan 2005 — Dec 2005

Education

Occupations

Scientist
Research Associate
Counselor
HR Specialist
Recruitment
IT Professional
Data Entry Specialist
Research Specialist
Research Scientist
Advisor
Data Scientist

Skills

Clinical Research
Login