Clinical Research Project Coordinator
3 settimane fa
We are seeking a skilled Clinical Research Coordinator to support our site in Italy.
This part-time role is for 24 hours per week and is expected to last approximately 12 months.
The primary responsibilities of the Clinical Research Coordinator will include maintaining accurate and up-to-date study protocols, case report forms, and electronic data capture systems.
Additionally, the successful candidate will be responsible for planning and coordinating logistical activities for study procedures, data entry, and data quality checking.
As a pivotal member of the site team, the Clinical Research Coordinator will assist in study enrollment, recruit, screen, and orient volunteers according to the study protocol.
The ideal candidate will possess a BS/BA in life sciences or an educational equivalent, along with relevant work experience in a clinical environment or medical setting.
Strong knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol, and study-specific operating procedures, consent forms, and study schedules is required.
The successful candidate will also have basic knowledge of medical terminology, strong IT competence, and excellent interpersonal skills.
We are looking for a fluent Italian speaker with good English language skills to join our team at IQVIA.
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