Alessia di Fusco
Senior Site Management Associate @ICON plc
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WORK HISTORY
Senior Site Management Associate @ICON plc
Responsible for managing, implementing and monitoring clinical studies, in a team setting according to ICON SOPs & Working Practices, applicable regulations and the principles of ICH-GCP. • The responsibilities of this position include, but are not limited to: identifying, training/initiating and closing out study sites; conducting remote site monitoring visits and/or targeted on-site visits as needed, conducting remote site management activities, managing study sites, assuring that data is reported accurately, and timelines are maintained. • Involved, when required, in other areas of study management and staff training and contribute to the review of ICON systems and procedures as appropriate. • Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues.
EDUCATION
Liceo Scientifico Statale "L. da Vinci", Vairano Patenora (CE)
P.N.I. Piano Nazionale Informatico
Università degli Studi del Sannio-Benevento
Master's degree, Genetics Science and Technology
ICON LMS
CTM Academy
Missione CRA (CRAsecrets.com, Yghea CRO)
48-hour clinical research training course in compliance with the Ministerial Decree 15.11.2011
Seconda Università degli Studi di Napoli
Bachelor's degree, Biological Sciences
SKILLS
ABOUT ALESSIA DI FUSCO
Senior Site Management Associate with 9+ years of experience in clinical research, specializing in observational studies on drugs and medical devices. Skilled in site management in Italy and abroad across multiple therapeutic areas (included but not limited to Oncology, Hematology, Rare Diseases) from selection to close-out. Experienced in on-site and remote monitoring, investigator meetings (including as speaker), audits, informed consent adaptation, contract negotiation, regulatory submissions, site payments, and data entry. Proven track record of delivering high-quality results and recognized for performance. LEGALLY PROTECTED STATUS UNDER ITALIAN LAW 68/99 CAREER GOAL Seeking a permanent, full-time, remote role as Clinical Trial Manager/Lead with minimal travel requirements.
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