ADVANCED ACCELERATOR APPLICATIONS
- Clinical research associate
SAINT-GENIS-POUILLY2015 - 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
Genève2013 - 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
Paris2009 - 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.
- 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)
