Research Nurse/Clinical Research Coordinator (Part-time, On-site, Independent Contractor) Nov[...]

RapidTrials; Novara; In loco; EUR 30.000 - 50.000; Part-time

Descrizione del lavoro

A clinical trial organization in Novara, Italy, is seeking a part-time Research Nurse/Clinical Research Coordinator to support prescreening and recruitment for a Phase III clinical trial. Responsibilities include engaging participants, coordinating procedures, and ensuring compliance with all regulations. The ideal candidate is a licensed nurse with at least 2 years of related experience, fluent in Italian and proficient in English. This freelance role requires a commitment of 20 hours per week for 6 months, with a potential extension.

Competenze

• Minimum 2 years’ experience as a research nurse and clinical research coordinator.
• Demonstrated prescreening/recruitment experience, preferably in metabolic/liver studies.
• GCP certification within the past 2 years required.

Mansioni

• Search EMR for potential participants.
• Coordinate and contact referral sources.
• Enter data into EDC.

Conoscenze

Research nurse

Clinical research coordination

Patient recruitment

Attention to detail

Communication skills

Fluent in Italian

Conversational English

Formazione

Licensed, university-educated nurse

Strumenti

EMRs

EDC

Clinical trial systems

Descrizione del lavoro

Research Nurse/Clinical Research Coordinator (Part-time, On-site, Independent Contractor) Novara Italy

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 Novara. 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: Novara, Italy

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
• Coordinate and contact referral sources
• Review patient charts/EMRs for eligibility
• Review patient lists
• Send appointment reminders
• Organize and assist with transportation and follow‑up

Patient Visits and Procedures:

• Vital signs
• Blood draws

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
• Valid professional license/registration in Italy

Qualifications & Requirements

• Licensed, university‑educated nurse
• 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 and conversational in English; proof of proficiency may be required
• Currently live and able to commute to a site located in Novara, Italy

Seniority Level

Mid‑Senior level

Employment Type

Contract

Job Function

Health Care Provider