Experience

Coalition PLUS

• France
• Non-profit Organizations
• 1 - 100 Employee

• Manager, Community-based Research Department

  • Mar 2018 - Present

  - Management of the Community-based Research team (6 Research Officiers, 2 Coordinators, 1 Biostatistician, and 1 Data Manager)- Support the Community-based Research Department Director in the management activities and representation- Coordination and participation in the valorisation of research projects (presentation at national and international conferences, scientific publications)- Participation in the development of a scientific and strategic technical support program for Coalition PLUS member associations for their research activities Show less

• Research Associate

  • Nov 2017 - Feb 2018

  - Implementation and management of research projects (drafting of the protocol, submission to the ethics committee, coordination of data collection, analysis, scientific valorisation)- Capacity building in community-based research within the structure and with partners (national or sub-region)- Literature review



AIDES

• France
• Civic and Social Organizations
• 300 - 400 Employee

• Research Officer (Chargée de Mission)

  • Nov 2016 - Nov 2017

  - Coordination a large, European community-based survey Flash! PrEP in Europe - Scientific reporting and presentation of findings at international and national scientific conferences - Literature review - Coordination a large, European community-based survey Flash! PrEP in Europe - Scientific reporting and presentation of findings at international and national scientific conferences - Literature review



INSERM

• France
• Research Services
• 700 & Above Employee

• PhD Graduate (Epidemiology)

  • Nov 2012 - Mar 2016

  Thesis title: Hemagglutination inhibition antibody titer as a correlate of protection against influenza infection: impact and dynamic- Conducted literature review, analysis and drafting of manuscript for two articles published in international, peer-reviewed journals - Participation and presentation (poster and/or oral) of preliminary findings at international conferences, research unit meetings, and doctoral school seminars - Examined the role of HI titer as a correlate of protection in the context of a single infection and considered the effect of repeated exposures on the immune response.- HI titer was studied among 167 covariates in an exploratory analysis to identify determinants of A(H1N1)pdm09 infection using data from a French cohort of 601 households (1450 subjects) representative of the general population. - Relationship between HI titer and protection against natural seasonal 2007 A(H1N1) infection was explored in an age-adjusted logistic regression model; longitudinal analysis explored the persistence of antibody titer following infection in a cohort of over 500 subjects Show less

• Clinical Research Associate/ Coordinator

  • Apr 2010 - Oct 2012

  - Assisted the project manager in the coordination and management of an observational study investigating risk factors of H1N1pdm09 in a cohort of 601 French households (1450 subjects)- Facilitated communication between study nurses, households and transporters to assure study protocol, visit schedules and specimen transport delays were respected- Study questionnaire development and data management of study visits- Verification of informed consent and training of study nurses on good clinical practices- Oversaw management and follow-up of study nurse contracts and payments - Participated in drafting of study protocol amendments and executed submission to regulatory authorities Show less



PPD

• United States
• Research Services
• 700 & Above Employee

• Clinical Research Associate II

  • Oct 2007 - Mar 2009

  - Initiation (project set-up) and management of a phase IIb lymphoma study at 9 investigational sites in France- Participation in the evaluation of the project budget, preparation of contracts and management of investigator payments- Responsible for training site staff on study protocol and guidelines- Performed regular visits on site for monitoring purposes, ensured timely completion and follow-up of monitoring reports- As primary French study contact, assured coordination between investigation sites, PPD project team, sponsor and central laboratories Show less

• Clinical Research Associate I

  • Jun 2006 - Oct 2007

  - Primary contact for three french investigational sites in phase III breast cancer trial- Primary French study contact for phase III osteopenia trial- Responsible for the study protocol training and monitoring at several participating French hospitals - Assured regular communication with sponsor for updates on study progress at site level- Oversaw investigational site compliance with French and FDA regulatory authorities

• Research Assistant

  • Dec 2005 - Jun 2006

  - Assisted Clinical Research Associates for two international phase III trials- Provided administrative support for study set up, data entry and document tracking- Maintenance and filing of study documents following company or sponsor SOPs.- Assisted Clinical Research Associates on site evaluation, monitoring, audit and close out visits.



Massachusetts General Hospital

• United States
• Hospitals and Health Care
• 700 & Above Employee

• Clinical Research Assistant II

  • Sep 2003 - Jul 2004

  - Patient enrollment in over ten investigator-initiated HIV/AIDS clinical trials (for the Partners AIDS Research Center), as well as one study run by the Centers for Disease Control (CDC) - Responsable for patient recruitment, screening and obtaining informed consent - Obtained blood samples (phlebotomy) - Development of case report forms - Design and maintenance of clinical databases - Assured upkeep of study regulatory binders - Patient enrollment in over ten investigator-initiated HIV/AIDS clinical trials (for the Partners AIDS Research Center), as well as one study run by the Centers for Disease Control (CDC) - Responsable for patient recruitment, screening and obtaining informed consent - Obtained blood samples (phlebotomy) - Development of case report forms - Design and maintenance of clinical databases - Assured upkeep of study regulatory binders



TIMI / PERFUSE Angiographic Core Laboratories

• Clinical Research Associate

  • Jun 2002 - Sep 2003

  - Lead angiographer for the CLARITY- TIMI 28 trial, funded by Sanofi-Aventis and Bristol-Myers Squibb - Lead angiographer for the phase 3 trials of CARDIOsphere®, sponsored by POINT Biomedical Corporation - Conducted the quantitative analysis of patient angiograms - Correspondence with study sites and sponsors - Assisted Director with design of study CRFs, Manual of Operations and Standard Operating Procedures - Lead angiographer for the CLARITY- TIMI 28 trial, funded by Sanofi-Aventis and Bristol-Myers Squibb - Lead angiographer for the phase 3 trials of CARDIOsphere®, sponsored by POINT Biomedical Corporation - Conducted the quantitative analysis of patient angiograms - Correspondence with study sites and sponsors - Assisted Director with design of study CRFs, Manual of Operations and Standard Operating Procedures