Denise A. Wright

CRS:

JHU

Role:

Research Staff

Position:

Data Manager/Regulatory Coordinator

Email:

dwright@jhmi.edu

Denise A. Wright has more than 20 years experience working with the Johns Hopkins ACTU, and is currently the Data Manager and responsible for Regulatory Affairs for ACTG and HPTN protocols. Ms. Wright oversees the CRS Data Management and Quality Assurance Team for all Network protocols.

Categories

Leadership Committees
CRS
Roles

Clinical Trials

A5128: Consent for Use of Stored Patient Specimens for...

The purpose of this study is to obtain informed consent to use stored human biological materials (HBM) (e.g., blood and other...

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P2005: A Phase I/II Open-Label, Single-Arm Study to Evaluate...

This study is currently on hold. The study is designed to characterize the pharmacokinetics of DLM using a model-based...

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P2010: Phase III Study of the Virologic Efficacy and Safety...

IMPAACT 2010 is a Phase III, three-arm, randomized, open-label study of HIV-1-infected pregnant women initiating either a...

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P2026: Pharmacokinetic Properties of Antiretroviral and...

IMPAACT P1026s, the predecessor of this study, was first approved in 2003. P1026s enrolled over 1000 pregnant/postpartum women,...

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A5361s: Pitavastatin to REduce Physical Function Impairment...

A5361s is a prospective study to determine the effects of pitavastatin on physical function. The study will enroll participants...

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