CLINICAL RESEARCH STUDY COORDINATOR > clinical-instrument data research from source documents> compiling the data collection database> compiling documents for clinical trialMEDICAL WRITING> collaboration in drafting protocol form AIFA2018 grant application> compilation of documents for project submission> collaboration in drafting clinical study protocol for HORIZON2020 grant application

STUDY START-UP for ASPYRE-1 STUDY (observational, multi-centre) & > planning of regulatory documentations> regulatory documentation submission to Ethics Committees satellite, > revision of informed consent forms > responsible as the contact for communication and interaction with companies and other investigatorsSTUDY COORDINATOR FOR CTEPH-SOLUTION PROTOCOL > collaboration as the contact for communication and interaction with companies and other investigatorsSTUDY COORDINATOR FOR RAMSES CLINICAL TRIAL (phase IV)> clinical-instrument data research from source documents> compiling the data collection database > compiling of documents necessary for clinical trialMEDICAL WRITING> English translation of the study protocol for RIO-COPD study

STAGE IN CLINICAL TRIAL CENTER UNIT - 'SAPIENZA' UNIVERSITY OF ROME ETHICS COMMITTEE> Validation process and organization of clinical trial documentation for ethics Committee submission> Validation process of clinical trial amendments

Collaboration for seminars and exams of Psychobiology and Behavioral genetict

Studying molecular and behavioral mechanisms involved in emotional memory, in psychopathology (i.e. PTSD, anxiety disorders) and in neurodegenerative disease (i.e. Alzheimer's disease, Tauopathies): • Investigating the role of orbitofrontal cortex in re-evaluation of traumatic experience; • Analyzed the role of miR34 in anxiety; • Behavioral analysis in mice expressing mutant TAU protein.

Investigating the expression of ERK protein in mouse loss Ras-GRF1: • Analyzed protein expression (Western Blotting); • Administrating central inhibitory drug (Stereotaxic surgery).