Research Nurse​/Clinical Research Coordinator; Part-time, On-site, Independent Contractor

Position: Research Nurse/Clinical Research Coordinator  (Part-time, On-site, Independent Contractor)
POSITION SUMMARY

Rapid Trials is hiring an experienced Clinical Research Coordinator (CRC) to support prescreening and recruitment activities for a Phase III MASH (Metabolic Dysfunction-Associated Steatohepatitis) clinical trial. This part-time, freelance role is based in Naples. The role involves identifying potential participants, engaging referral sources, coordinating prescreening, assisting with completing patient procedures during study visits and ensuring compliance with protocol, GDPR, and site SOPs.

Role Type:
Onsite

Location:

Naples
Contract Type:
Independent Contractor / Freelance
Duration: 6 months with potential for extension

Hours:

20 hours per week
Total Project

Hours:

520

Reports To:

PI or Designee

KEY RESPONSIBILITIES
Prescreening & Recruitment
Search EMR for potential participants
Contact referral sources
Coordinate with referral sources
Review patient charts/EMRs for eligibility
Review patient lists

Patient & Referral Engagement
Send appointment reminders
Organize transportation
Assist with transport and follow-up
Patient Visits and Procedures
Blood draws
Vital signs
Documentation & Systems
Enter data into EDC
Review and QC data in EDC
Maintain accurate and compliant documentation per site, sponsor, and hospital SOPs

Compliance & Training
Complete onboarding requirements:
-   Training on protocol and study-related tools and systems
-   Site Training, including SOPs and workflow
-   Ensure GDPR-compliant data handling, including consent for background checks and data usage
-   EU work authorization and freelancer eligibility (tax , self-employment registration)
-   GCP certification within the past 2 years required
-   Criminal record certificate (national) required
Immunization/health records/clearance (Hep B, MMR, Varicella, TB, COVID-19)

QUALIFICATIONS & REQUIREMENTS
Licensed, university-educated nurse
-Valid professional license/registration in Italy
Minimum 2 years’ experience as a research nurse and experience as a clinical research coordinator
Demonstrated prescreening/recruitment experience, preferably in metabolic/liver studies
Proficiency with EMRs, EDC, and clinical trial systems
Prior experience with industry-sponsored trials, strongly desired
Strong attention to detail, independent work ethic, and excellent communication skills
Fluent in Italian (site language) and conversational in English; proof of proficiency may be required
Currently live and able to commute to a site located in Naples, Italy