Clinical Research Associate (CRA)
Since April 2015
Site opening visits, monitoring visits and closeout visits; Verification of informed consent and Investigator files; verification of CRF and original documents (SDV); Clinical site support: phone contacts, email contact, follow-up letters; Violations of the Protocol, report deviations to the protocol Monitoring of electronic CRF (if applicable); monitoring reports, support for adverse event reporting; support to researchers in the preparation of reports to the Ethics Committees Study progress reports and compliance metrics.
Clinical Research Associate Trainee
October 2014 --- March 2015
Obtained Certified as CRA according to Italian D.M. 15th November 2011.
December 2013 --- September 2014
Worked , with a large team of pharmacists, as galenic drugs preparer and as pharmacist.
June 2012 --- March 2013
Educational training program.
Master degree in Ethical, regulatory and methodological aspects in clinical trials from Università di Roma Tor Vergata in 2014
Degree in pharmacy from Sapienza Università di Roma in 2013
Scientific high school diploma in from i.t.a.s. Colomba Antonietti di Roma in 2008
Qualification to the pharmacist profession in from Sapienza Università di Roma in 0
Training and Certification