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10 years of experience working in the Clinical Research field in the US, Puerto Rico, Mexico and EU. Certification in Project Management (Prince2 Practitioner). Key Competencies: • Coordinate/manage operational activities for international multi-center Clinical trials Phase II-IV, several therapeutic areas, from set-up to close-out. • Lead cross-functional meetings to keep each team member informed on study progress/key project deliverables • Complete feasibility studies and sites selection • Prepare and submit ethics/regulatory packages • Ensure all sites are in compliance with the study protocol, ICH/GCP guidelines, FDA and local government regulations • Initiate improvements to enhance the efficiency and the quality of the work performed on assigned projects • Prepare audit and follow through until resolution of findings • Propose and implement action plans, as needed • Track progress of / assist with data cleaning activities • Provide trial-specific trainings, conduct co-visits • Train and mentor new team members Additional skills include: • Effective verbal & written communication skills • Ability to work cooperatively and independently • Ability to plan proactively to ensure project deliverables are met • Ability to rapidly adapt to changes Thrilled by new opportunities. Passionate about innovation in Public Health and Global Health. Therapeutic Areas include : Mental Disorders (Major Depressive Disorder, Schizophrenia), Urology (Chronic Kidney Disease, Overactive Bladder Syndrome), Endocrinology (Diabetes, Obesity), Infectious Diseases (Influenza, Acute Otitis Media), Hematology (Iron Overload), Musculoskeletal (Osteoporosis).


Past Experience

  • Senior/ Lead Clinical Research Associate - New York City (USA)
    January 2014 --- January 2015
    Management & Monitoring of assigned sites across United States & Puerto Rico. Mentoring of Junior CRA. Therapeutic areas: CNS, Infectious Diseases

  • Clinical Research Associate - New York City (USA)
    January 2008 --- January 2014
    Management & Monitoring of assigned sites across United States, Puerto Rico and Mexico. Therapeutic areas: CNS (pediatrics), Infectious Diseases

  • Clinical Research Associate - Paris (France)
    January 2006 --- January 2008
    Sites management in France and Belgium (Wallonia and Flanders regions) in International Phase II and III trials including preparation and submission of regulatory documents to EC and Regulatory Authorities, initiation, monitoring and close-out visits. Therapeutic areas: Hematology, Urology, Gastrointestinal, Endocrine/Metabolic

  • Clinical Research Associate - Paris (France)
    February 2006 --- April 2006
    Responsible for contacting over 500 sites in France for sites selection and database management for Phase IV studies. Therapeutic area: CNS


LinkedIn Assessment :
Clinical trialsEDCClinical researchICH-GCPTherapeutic AreasProtocolClinical monitoringInformClinical DevelopmentPediatricsFDAPatient SafetyPatient recruitmentCROPharmaceutical IndustryInternational RelationsLife SciencesDiabetesGCPInfectious diseasesEndocrinologyCTMS


  • in Project Management PRINCE2 Certification from Cegos (Paris) in 2016
  • Certified Clinical Research Coordinator in Pharmaceuticals from Clinact (Paris) in 2006
  • Master of Public Health (MPH) in Université Claude Bernard (FR)/Universiteit Utrecht (NL) from Université Claude Bernard (Lyon I) in 2006
  • MSc in Metabolism, Endocrinology and Nutrition from Université Claude Bernard (Lyon I) in 2005
  • BSc in Animal physiology, pharmacotoxicology and biochemistry from Université Paul Sabatier (Toulouse III) in 2004

Training and Certification

  • Project Management (Prince2 Practitioner) Certification

Area / Region

Paris, France


Driving License
  • Yes