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CV créé le : 27/09/2023
CV modifié le : 27/09/2023
Dernière connexion : 10/10/2023
Coordonnées
********** ********

Adresse :

Rueil-Malmaison (92500)
Email : **********.********@*******.**
Port. : ************
Clinical Research Associate, Confirmé
Référence : 687581
Expériences Professionnelles
nov. 2021 Clinical Research Associate
Parexel International/Paris, Ile-de-France, France
* Clinical sites' main point of contact, accountable for quality and delivery of sites from Site selection to Closeout
of the trial.
* Oversees the conduct of the trial at designated sites and ensures rights and well-being of human subjects
* Facilitates and supports sites with access to study systems and ensures sites are compliant with project
specific requirements and according to the ICH-GCP regulations and SOPs.

nov. 2019 oct. 2021 Clinical Research Associate
PRA Health Sciences/Levallois-Perret, Ile-de-France, FRANCE
* Responsible for all aspects of study site monitoring, including routine monitoring and close-out visits, maintenance of
study files, conduct of pre-study and initiation visits, liaise with vendors
* General On-Site and Off-Site Monitoring Responsibilities, travel, including air travel
* Pharmacy visits: verified reception, dispensing and storage conditions of study drugs
* Performed CRF review, query generation and resolution against established data review guidelines, on PRA or client
data management systems
* Updated, tracked and maintained study-specific trial management tools/systems
* Tracked and follow-up on serious adverse events
* Followed aspects of SOPs and ICH-GCP

mai 2019 nov. 2019
PRA Health Sciences/Levallois-Perret, Ile-de-France, FRANCE
* Performed study tracking via CTMS or Sponsor designated system
* Performed essential document collection, review, maintenance and close-out activities
* Supported investigators and investigative staff in fulfilling obligations with regard to local submissions according to
local regulatory and Institution Review Board (IRB)/Independent Ethics Committee (IEC) requirements

juil. 2018 avr. 2019 Clinical Research Associate / Study Coordinator
Hôpital Raymond Poincaré - APHP/Garches, Ile-de-France, FRANCE
* Performed on-site initiation and monitoring visits
* Verified informed consents forms, reported of Serious Adverse Events, checked quality of data
* Pharmacy visits: verified reception, dispensing and storage conditions of study drugs
* Followed-up with patients by phone or face-to-face interviews
* Collected clinical data from patient source files

déc. 2017 juin 2018 Clinical Research Associate Trainee
KEYRUS BIOPHARMA/Levallois-Perret, Ile-de-France, FRANCE
* Collected data into eCRF and performed on-site and remote monitoring, wrote visit reports

oct. 2016 juin 2017 Research Engineer
INSERM U1195/Le Kremlin-Bicêtre, Ile-de-France, FRANCE
* Studied cerebroprotective effects of neurosteroids after ischemic stroke by animal experiments (mice breeding,
intraperitoneal or intravenous injections, blood samples/tissues)

janv. 2016 juil. 2016 Research Engineer trainee
CEA - COMMISSARIAT À L'ÉNERGIE ATOMIQUE ET AUX ÉNERGIES ALTERNATIVES, Fontenay-aux-Roses, Ile-de- France, FRANCE
* Studied the role of mast cells in cognitive alterations in Alzheimer's disease by mice experiments (brain perfusion
and anatomic Magnetic Resonance Imaging, mice breeding and behaviour tests)

janv. 2015 avr. 2015 Research Engineer trainee
INSTITUT GUSTAVE ROUSSY/Villejuif, Ile-de-France, FRANCE
* Established a cellular model for a rare hereditary disease, Birt-Hogg-Dubé disease (human cell culture, CRISPR/Cas9
genome editing technique

Therapeutic Experience
* Intensive care/COVID-19 Acute Respiratory Distress Syndrome (III)
* Dermatology/ Chronic Hand Eczema (III)
* Gastroenterology/Short Bowel Syndrome (II)
* Oncology/Solid Tumors/Multiple Solid Tumors (I)
* Oncology/Solid Tumors/Renal Cell Carcinoma (I/II)
* Neurology/Pain/Migraine (IIB)
* Oncology/ Non-small-cell lung carcinoma - NSCLC (III)
* Oncology/Solid Tumors/Ovarian cancer (III)
* Neurology/epilepsy, physical medicine/lateral epicondylitis, hemiplegia after stroke (III)
* Hematology/Leukemia/Acute Myeloid/Myelogenous-AML (III)
* Surgical/Volume Depletion/Hypovolemia (IV)
* Nephrology (IV)
* Cardiology/Surgical/Intraoperative Bleeding (IV)

Language
* French (native language)
* English (fluent)
* Creole (advanced)

Diplômes et formations
sept. 2017 Certified Clinical Research Associate (CCRA), For Drug Consulting
Malakoff, France

juil. 2017 University Diploma - Translational Research
University of Paris-Sud, Orsay, France

juin 2017 Master's degree in biology of aging - BAC+4
University of Paris Saclay, Versailles Saint-Quentin-en-Yvelines, France, Mar

juil. 2014 Bachelor of Science (B.Sc) in biology - BAC+3
Versailles Saint-Quentin-en-Yvelines, France

Compétences
data management systems, Excel, PowerPoint, Word, Open Office, clinical data, CTMS, Vault
Compétences linguistiques
Anglais
Français
Important
CV actualisé il y a plus de 6 mois, certaines informations peuvent ne pas être à jour.
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