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Q&A With Leslie Henderson-Williams

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Leslie Henderson-Williams
Manager, Clinical Operations, Quintiles, Inc

Location: Parsippany, NJ United States
Joined: Jul 27th, 2022
About   (request update)
Education   (request update)
Hampton University class of 1989
Undergrad Major: Biology
- College Not Listed - class of 2001
Grad Major: Biology
Experience
I currently work with Quintiles, Inc as Manager, Clinical Operations
I have years of experience working in the Biotechnology and Pharmaceutical industry.
Manager, Clinical Operations | Quintiles, Inc
From June 2008 to Current • 18 year(s)
Line management of CTLs in the North East, coordinating client communications, monitoring regulatory status, and overseeing site management and clinical monitor performance.
Clinical Study Manager | Quintiles, Inc
From April 2007 to June 2008 • 1 year(s)
Accountable for planning and delivery of clinical components of large, complex protocols and global projects, leading teams of CTLs across projects.
Clinical Scientist | Quintiles, Inc
From June 2004 to April 2007 • 3 year(s)
Managed clinical teams for multicenter global clinical trials, overseeing site identification, study start-up procedures, and ensuring adherence to GCP/ICH guidelines.
Manager of Clinical Research Education | Association of Clinical Research Professionals (ACRP)
From May 2003 to June 2003 • 0 year(s)
Responsible for development and implementation of training programs, particularly scientific aspects, and establishing/meeting deadlines for educational materials.
Senior Clinical Trial Manager | Omnicare Clinical Research, Inc
From October 2002 to April 2003 • 1 year(s)
Established positive client interactions with Sponsors, provided direct line management to field-based employees, and managed 15 field-based CRAs on large Phase III trial.
Associate Director, Clinical Operations | Quintiles, Inc
From February 1999 to September 2002 • 3 year(s)
Developed cost estimates, monitored budgets, performed task delegation and supervision, and coordinated communications with clients and project teams.
Senior Clinical Research Associate | Warner-Lambert Company
From April 1996 to December 1999 • 3 year(s)
Responsible for pre-study, initiation, monitoring, study design, planning, and closeout procedures for Phase I-IV clinical studies, serving as project manager for multiple trials.
Clinical Research Associate | Whitehall-Robins Healthcare
From December 1993 to March 1996 • 3 year(s)
Project team leader for Phase III Analgesic clinical trial, trained investigators and study staff, and maintained timely documentation of clinical study progress.
Clinical Research Associate | In Vivo, Inc
From December 1992 to December 1993 • 1 year(s)
Responsible for coordination of clinical drug studies, served as liaison between study sites and sponsors, and ensured integrity of study data collected in the field.
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