Clinical Research Coordinator (Clinical Trials)

Location: Rome, Roma, Italy; onsite clinical research site

Salary: €29,800–€44,800 annualized, with the actual amount dependent on qualifications, location, and schedule.

Company

A global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Perform prescreening and screening activities and support patient enrollment.
• Review charts from the site database and maintain study documentation, including protocols, case report forms, and electronic data capture systems.
• Support informed consent and privacy documentation.
• Coordinate logistical activities for study procedures in accordance with the study protocol.
• Communicate with study monitors, respond to study-related inquiries, and complete general administrative tasks.

Requirements

• Bachelor’s degree in life sciences or equivalent education and/or relevant clinical or medical experience.
• At least 2 years of experience as a Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator at a clinical trial site.
• Solid understanding of clinical trials, study protocols, consent forms, and study schedules.
• Good knowledge of medical terminology and strong proficiency with Microsoft Office applications, including Outlook, Word, Excel, and Access.
• Excellent interpersonal, communication, organizational, and attention-to-detail skills.
• Fluency in English required.

Culture & Benefits

• Part-time schedule of 2 hours per week.
• Approximately six-month engagement starting immediately.
• Supportive and collaborative work environment.
• Opportunity to contribute to clinical research and healthcare development.
• Health and welfare benefits may be available depending on the position and compensation arrangement.