Desiree Nock-Chester




Research Staff


Research Assistant


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.


Leadership Committees

Clinical Trials

A5300/P2003: PHOENIx Feasibility Study

Study of MDR TB Cases and Their Household Contacts: Operational Feasibility to Inform PHOENIx Trial Design

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A5225: Phase I/II Dose-Finding Study of High-Dose...

A5225/HiFLAC is a Phase I/II dose escalation and validation study of the safety, tolerability, and therapeutic effect of an...

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P1060: Phase II, parallel, randomized, clinical trials...

P1060 is currently at protocol Version 5.0, which is an extension phase of P1060 Version 4.0. P1060 Version 4.0 was a Phase II,...

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A5288: MULTIOCTAVE, Management Using the Latest Technologies...

The study is being done to: test a strategy of using a resistance test to choose anti-HIV drugs. Resistance tests look at the...

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P1073: Study of Immune Reconstitution Inflammatory Syndrome...

P1073 is a case controlled prospective, clinical, observational and pathogenesis study of HIV-infected infants and children...

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