Alberto Calabrò

Coordinate global Compassionate Use and Pre approval access programs for selected Roche molecules.

My primary responsibility lies in the supervision of clinical research trials with specific attention to patients safety, protocol adherence, quality of generated data and respect of time lines.

A Research Assistant is responsible for providing project administrative support to Clinical Team Managers, Project Managers and/or CRAs on designated project teams. Responsible for all administrative aspects of allocated studies, including file maintenance and trial tracking input.

As Pre- Doctoral fellow, I was in charge of my own research project. The duties related to such position cover both practical and organizational aspects. The first ones are related to the protocol development and data analysis, the second one instead are more directed towards budget, time management and collaborators coordination. The last part of the PhD studies is usually dedicated to writing and summarizing for the scientific community the research carried on in the previous years.

As guest scientist my duties were addressing the scientific development of several protocols for the general use of the laboratory.

As graduate student in the laboratory where I studied for my master degree, I was responsible for the summer school students and to complete part of the experiments related to the research topic performed at that moment in the laboratory.

Human breast cancer