Desiree Nock-Chester

CRS:

JHU

Role:

Research Staff

Position:

Research Assistant

Email:

dnock1@jhmi.edu

Desiree Nock-Chester responsible for QA/QC. Her duties include QA/QC of charts and crf binders, visit prep, creating laboratory requisitions, resolving queries and delinquencies, transcription, data entry, and maintaining error reports.

She has been a part of the data staff of the ACTG  at Johns Hopkins University for more than 10 years. She began as the transcriptionist for the unit and held that position for nearly 3 years. Prior to joining the clinical trials unit, Ms. Nock-Chester worked in the Wilmer at  Johns Hopkins for 9 years as a Sr. Patient Services Coordinator. Her  duties included registering patients for appointments, surgeries, post-op visits, verifying insurance information, obtaining referrals, and balancing out the daily intake of co-payments.

Categories

Leadership Committees
CRS
Roles

Clinical Trials

A5322: Long-Term Follow-up of Older HIV-infected Adults in...

The A5322 protocol is a long-term observational study, with a planned series of analyses of data to be collected from an...

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A5342: Evaluating the Safety, Tolerability, and Effect of a...

The purpose of this study is to evaluate the safety, tolerability, and effect of an experimental human monoclonal antibody...

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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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A5329: Interferon –Free Therapy for Chronic Hepatitis C...

A5329 is a study for people who are infected with both HIV and the Hepatitis C virus (HCV) and have never taken Hepatitis C...

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A5349: Rifapentine-containing treatment shortening regimens...

The purpose of this study is to determine whether one or two four-month regimens of tuberculosis treatment are as effective as a...

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