Milan, Lombardy, Italy
Clinical Research Associate dedicated to Johnson&Johnson Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. • Building and mantaining effective relationship with site personnel and stakeholders to facilitate smooth trial operations.
Clinical Research Associate dedicated to Bayer •Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting. • Building and mantaining effective relationship with site personnel and stakeholders to facilitate smooth trial operations.
-management of the ideal setting for reliable data production (volounteers enrollment according to the inclusion/exclusion criteria and the timeliness in the experimental protocol) -evaluation of the quality of the data collected -follow up on the protocol drafting project -allignment and verification of data collected during ongoing experimentation -statistical anaysis (R software, excel) of the data
The aim of my work was to assess the effects on fibrosis of HDAC inhibitors in a model of cardiomyopathy in dystrophic mice
Hostess during events and promoter for different food products and brands