Experience

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  Institut de la vision

  Nov 2015 - May 2016

  Research trainee

  As part of the validation of my DUT in Biological Engineering, option Biological and Biochemical Analyses at the IUT of Bobigny, I did a 6-month internship, from November 16, 2015 to May 16, 2016, at the Institut de la Vision. I was welcomed in Deniz DALKARA's team entitled "Gene therapies and animal models for neurodegenerative diseases" and worked on the thesis project of Hanen KHABOU, PhD student on the following subject "Retinitis Pigmentosa: gene therapies to prevent and restore vision".Retinitis Pigmentosa is a degenerative disease of the retina which can lead to blindness in its late stages. Thus, the aim of this gene therapy project was to succeed in preventing and restoring the loss of central vision in the long term thanks to the combined expression of 1) RdCVF (Rod derived Cone Viability Factor), a neurotrophic factor that preserves cones; and 2) halorhodospin, a protein that restores cone activity, which is progressively lost during the development of the disease when it is not treated. My supervisor did all the in vivo part. I therefore helped her to prove that these therapies have a preventive and curative effect on this disease using different techniques: -Immunolabelling of cones on treated retinas -Counting and comparing the number of photoreceptors in the retina -RT-qPCR to measure the level of gene expression-RNA extraction-Extraction of retina from mouse eye-Statistics Show less

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  Institut mondor de recherche biomédicale

  May 2017 - Jul 2017

  Stagiaire

  Dans le cadre de la validation de ma troisième année de licence Sciences de la Vie et de la Terre – Biologie Santé à l’UPEC, j’ai effectué un stage de 2 mois à l’Institut Mondor de la Recherche Biomédicale à Créteil. J'ai réalisé mon stage au sein du département « Virus, Immunité, Cancer » parmi l’équipe 18, INSERM U955, dirigée par le professeur Jean-Michel PAWLOTSKY. Nous y étudions « L’influence du microenvironnement inflammatoire dans la progression du carcinome hépatocellulaire (CHC) et dans la non-réponse aux traitements anti-cancéreux ». Show less

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  Hôpital saint-louis

  Dec 2017 - Mar 2018

  - Medical staff, Multidisciplinary Consultation Meetings.- Consultation with the doctor for pre-screening.- Typical days of a sutdy coordinator (Meeting and accompanying newly included patients during their various pre-inclusion examinations, preparation of biological samples to be sent to the sponsor laboratory, filling in the e-CRF, answering queries).- Meeting with a sponsor CRA during a monitoring visit.- Digitalisation of functional scores for the Quality Of Life study.- Search for missing items in the source files for the Voozanoo database.- Organisation of the first MATHEC day (creation of the brochure and badges, room reservation and organisation of the space, reception of participants).- Translation of the functional scores into Portuguese.- Helping with the translation between the medical team and a Portuguese patient. Show less

  • Junior study coordinator

    Mar 2018 - Mar 2018

  • Study coordinator Trainee

    Jan 2018 - Feb 2018

  • Laboratory Technician

    Dec 2017 - Dec 2017
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  Astrum cro france (formerly popsi cube)

  Apr 2019 - Dec 2019

  Clinical research associate outsourced to l'oréal

  Collection and entry of data from clinical study reports in Cosmetology.

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  Cerc (cardiovascular european research center)

  Jan 2020 - Jan 2023

  Driving the planning, coordination, and execution of domestic or international clinical trials in the medical device field Overseeing and preparing scientific documents (information to patients, case report forms) Preparing, critically reviewing, and submitting regulatory files Leading the organisation and management of study committees (CEC, DSMB) Managing and coordinating internal and external staff resources Supervising progress of monitoring activities Leading the project team, ensuring the projects are delivered according to planned scope and timelines Developing study-specific documentation Managing project study budgets and invoicing procedures according to study contract Planning, organization and presentation of Investigator's Meeting, Validation of site visit reports (site initiation, monitoring and close-out), Liaison with the CRAs for appropriate study site monitoring, Periodic feedback to the Client, Management of the Serious Adverse Events and other safety issues during the clinical study, Management of data collection and quality, Show less Project Manager:Driving the planning, coordination, and execution of domestic or international clinical trials in the medical device fieldOverseeing and preparing scientific documents (information to patients, case report forms)Preparing, critically reviewing, and submitting regulatory filesLeading the organisation and management of study committees (CEC, DSMB)Managing and coordinating internal and external staff resourcesSupervising progress of monitoring activitiesLeading the project team, ensuring the projects are delivered according to planned scope and timelinesDeveloping study-specific documentationManaging project study budgets and invoicing procedures according to study contract Planning, organization and presentation of Investigator's Meeting,Validation of site visit reports (site initiation, monitoring and close-out),Liaison with the CRAs for appropriate study site monitoring,Periodic feedback to the Client,Management of the Serious Adverse Events and other safety issues during the clinical study,Management of data collection and quality,CRA:Responsible for site management from initiation to close-out in accordance with study specific procedures, applicable SOPs, and ICH GCP guidelinesRemote monitoring via e-CRFTraining and information for investigators and the clinical studyPrivileged contact with investigators centersOn site monitoring of patient safety (review of SAEs, AEs)Generate visit reports in compliance with the monitoring planUpdate all relevant tracking systems on an ongoing basis Show less Responsible for site management from initiation to close-out in accordance with study specific procedures, applicable SOPs, and ICH GCP guidelinesRemote monitoring via e-CRFTraining and information for investigators and the clinical studyPrivileged contact with investigators centersOn site monitoring of patient safety (review of SAEs, AEs)Generate visit reports in compliance with the monitoring planUpdate all relevant tracking systems on an ongoing basisAssist the Clinical Project Leader in regulatory submissions when needed Show less

  • International Clinical Project Leader

    Dec 2021 - Jan 2023

  • Clinical Project Leader / Clinical Research Associate

    Apr 2021 - Dec 2021

  • Multilingual Clinical Research Associate

    Jan 2020 - Apr 2021
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  Roche

  Mar 2023 - now

  Medical evidence project specialist chez aixial pour le compte de roche