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Clinical research coordinator ( part-time)

Salerno
RapidTrials
Pubblicato il 16 marzo
Descrizione

POSITION SUMMARY


Si assicuri di leggere attentamente le informazioni relative a questa opportunità prima di inviare la sua candidatura.

RapidTrials 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

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 ID, self-employment registration)

- GCP certification within the past 2 years required

- Criminal record certificate (national) required

QUALIFICATIONS xjrgpwk & REQUIREMENTS

* Minimum 2 years' 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

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