Clinical Research Coordinator in Palermo
Working Hours: Part-time, 24h per week
Start Date: Immediately
Duration: Approximately 6 months
IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Palermo. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Key Responsibilities
* Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
* Supporting patient screening and enrollment, including handling informed consent and privacy documentation
* Coordinating logistical activities for study procedures in line with the study protocol
* Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
* Patient education
* Communicating with study monitors and responding to study-related inquiries
* Carrying out general administrative tasks related to the study
Your Profile
* Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
* Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
* Good knowledge of medical terminology
* Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
* Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
* Excellent interpersonal and communication skills
* Strong organizational skills and attention to detail
* Fluency in Italian and good command of English
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