Turin, Piedmont, Italy
Clinical Research Consultant with experience in dermatology and a strong background in infectious disease research, as a study coordinator. Extensive knowledge of GCP and GLP standards, with hands-on experience across Phase I–IV clinical trials. Proven expertise in collaborating with CROs and sponsors, coordinating study activities, and managing regulatory and study documentation. Currently working within a CRO environment, providing clinical research support and consultancy in dermatological studies.
Clinical Study Coordinator at Ospedale Amedeo di Savoia - Infectious Diseases - Coordinate Phase I–IV clinical trials in the field of infectious diseases. - Ensure compliance with Good Clinical Practice (GCP) and applicable regulations. - Support physicians and nurses throughout the study process. - Liaise with sponsors, CROs, and Ethics Committees. - Manage clinical trial documentation and agreements.
Clinical Study Coordinator at Ospedale Amedeo di Savoia - Infectious Diseases - Coordinate Phase I–IV clinical trials in the field of infectious diseases. - Ensure compliance with Good Clinical Practice (GCP) and applicable regulations. - Support physicians and nurses throughout the study process. - Liaise with sponsors, CROs, and Ethics Committees. - Manage clinical trial documentation and agreements.
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