Team-oriented senior Data Manager with extensive international experience managing clinical research studies in one the top 10 leading healthcare companies in the world, a high-growth medical devices company, as well as dynamic CROs. Demonstrated track record in leading high-profile data management clinical studies, SAS programming across a broad array of study types including Stage 1, 2 and 3 clinical trials and medical devices. Extensive international experience, strong communicator across all levels of organisations, detail-oriented, a self-learner and client-focused. More than 16 years of experience in clinical research, data management managing phase 3 cardiology and CNS studies, phase 1 in house studies, project management experience through subcontracted studies, medical devices experience, SAS programming in Diabetes and Osteo-arthritis.Very strong communication skills.Extensive international experience.
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Data Management Project LeadBiotrialHouston, Tx, Us -
Senior Clinical Data Manager And Sas ProgrammerProxima Clinical Research, Inc. Jun 2022 - Oct 2023Houston, Texas, United StatesClinical data management and SAS programmer.* Managed and delivered the data base design and data cleaning process using Medrio.* Updated and improved three pre-existing phase 3 studies and met clients’ deliverables and timeline requirements. * Created the SAS program sets, including 3 DSMBs, and a set of SAS edit checks, meeting the clients’ required deliverables and deadlines. -
Sas ProgrammerBiosplice Therapeutics May 2019 - Mar 2020Greater San Diego Area(Samumed)Managed all SAS programming requirement for Osteo-arthritis studies including:* Programmed SDTM datasets and graphs. * Created and submitted listings and tables, applying the latest SAS programming techniques, for data management data cleaning.* Designed and implemented the lab transfer system.* Designed and implemented the associated SAS programs across output programming.* Other team-support functions including: Programmed specification documents, Programmed an STDM.* Completed aADaM training at CDISC interchange in San Diego in 2019 and at PharmaSUG in 2019. -
Clinical Data AssociateDexcom May 2017 - Apr 2019Greater San Diego AreaManaged various SAS programming requirement for the Dexcom real-time continuous glucose monitoring device for diabetes management:* Created CRFs.* Designed and tested databases in Medrio, including ePRO forms and Redcap.* Created, edited and checked programming in EDC-Medrio and in SAS.* Studied discrepancy resolution in Medrio.* Studied outputs created including listings and summary tables and debugging of SAS programs.* Expertise in CSR creation, staff training and presenting study results. -
Sas Programmer, Biostatistics & ProgrammingSanofi-Aventis Feb 2009 - Mar 2015Frankfurt Am Main, Hesse, Germany* Managed all SAS programming requirement for the CEP therapeutics * Led Oracle-Clinical database designs* Managed all subcontracted clinical data management studies* Managed in-house clinical data management studies
Noudjoum Hibbert Education Details
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Molecular Modelling -
Organic Chemistry/Bio Molecules
Frequently Asked Questions about Noudjoum Hibbert
What company does Noudjoum Hibbert work for?
Noudjoum Hibbert works for Biotrial
What is Noudjoum Hibbert's role at the current company?
Noudjoum Hibbert's current role is Data Management Project Lead.
What schools did Noudjoum Hibbert attend?
Noudjoum Hibbert attended Faculté Des Sciences Aix-Marseille Université, University Of Montpellier.
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