Overview
Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Catanzaro.
Role scope: 24 hours per week and is expected to last approximately 3 months.
Responsibilities

Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.)
Planning and coordinating logistical activity for study procedures according to the study protocol
Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
Management and shipment of biological samples
Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
Administrative research task

Qualifications

BS / BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting (e.g., clinical research coordinator, Research Assistant, nurse, medical assistant, or other medical profession)
Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Basic knowledge of medical terminology
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
Good organizational skills with the ability to pay close attention to detail
Fluent Italian with good English language skills

Job Details

Contract types: Part-time, Contract
Contract length: 13 weeks
Pay: From €20.00 per hour
Expected hours: 24 per week
Work Location: In person

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