Clinical Research Coordinator
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Young professional with a strong motivation to learn and grow professionally in a business context.
During my work experience at the CRO in Aviano, I acquired excellent skills as a data manger and coordinator of observational and interventional phase I, II, III and IV clinical trials.
I honed my organizational, stress management, document review and data collection program (eCRF, TMF) skills.
Coordination and Conduct of interventional (Phase I, II III, IV) and observational Profit and non-Profit studies in accordance with Good Clinical Practice (GCP):
Start-Up Activities: preparation of documentation required for submission of clinical trials to Competent Authorities;
Management Activities: investigational drug, biological specimen shipments, data collection (electronic and paper CRFs), training patients on completion of study diaries, notification of serious adverse events, archiving documentation and updating Investigator Site File, supervision of all procedures required by the research protocol.
Regulatory Activities: communications to Competent Authorities Coordination of Study Staff and interface with the Operational Units involved in the conduct of the Clinical Trial (Scientific Management, Pharmacy, Laboratory) and with the Promoters.
Master, Pharmaceutical Managment : Medical Science Laison e Medical Advisor
PhD - Neurodegenerative diseases and Molecular nutrition - Ex vivo studies on Alzheimer's disease (AD), Parkinson's disease (PD) and cardiovascular disease (Gilbert syndrome).
Degree in Chemistry and Pharmaceutical Technology
