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Benoit MUSEL

SAINT-GENIS-POUILLY

En résumé

Mes compétences :
Recherche clinique
Bonnes Pratiques Cliniques
Essais cliniques
Monitoring

Entreprises

  • ADVANCED ACCELERATOR APPLICATIONS - Clinical research associate

    SAINT-GENIS-POUILLY 2015 - maintenant - Studies: Phase I/II, "ATU de Cohorte".
    - Medical fields: Oncology, cardiology, gastroenterology, nuclear medicine, rheumatology.
    - International monitoring: UK, Switzerland, Canada
    - Conduct on-site initiation, monitoring and close-out visits.
    - Manage investigational medicinal product and other study materials.
    - Planning, set-up and follow-up of the clinical trials. Participation in regulatory steps (e.g. submission to Competent Authorities and Ethics Committee).
    - Follow-up of study budgets in collaboration with project leaders.
    - Follow-up of the clinical trial progress. Follow-up of the subcontractors during the clinical trial (CRO).
    - Update of study documents (IB, IMPD), development of CRF and ICF. Participation in writing and reviewing clinical study reports (CSR) and statistical analysis plans (SAP).
    - Management and follow-up of investigator-sponsored trials.
    - Participation in protocol design, discussion with investigators.
    - Participation in CRO selection and audit.
    - Training of junior CRA.
  • Hôpitaux Universitaires de Genève - Clinical and basic research scientist

    Genève 2013 - 2014 - Development and coordination of scientific projects
    - Testing of brain damaged patients
    - Descriptive and inferential statistical analyses
    - Physiological analyses
    - Neuropsychological and neurophysiological testing’s
    – Magnetic resonance imaging (MRI) examinations and analyses
    - Scientific publications in international journals
    - Involvement national and international conferences
    - Student training
    - Search for public and private funding for scientific projects
    – Project planning and budgeting.
  • CNRS - Clinical and basic research scientist

    Paris 2009 - 2012 - Testing on patients with brain and eye lesions
    - Descriptive and inferential statistical analyses
    - Magnetic resonance imaging (MRI) examinations and analyses
    - Scientific publications in international journals
    - Involvement national and international conferences
    – Writing protocols and CPP
    – University teaching
    – Scientific animation
    - Student Training.

Formations

  • For Drug Consulting

    Malakoff 2015 - 2015 Clinical research associate

    - National and international regulations
    - Regulatory procedures
    - Good Clinical Practice (GCP / ICH)
    - Clinical trial methodology
    - Monitoring
    - Pharmacovigilance
    - Communication and reporting
  • Université Grenoble 2 Pierre Mendès France (Grenoble)

    Grenoble 2009 - 2012 Doctorat

Réseau

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