Clinical Research Associate FREELANCE

Overview

Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a :

Clinical Research Associate

To reinforce the Operational Italian Team

Responsibilities

• Conduct and perform SQV / Pre-study Visits, site initiation visits, monitoring visits, close out visits, according to SOPs and study Monitoring Plan
• Handle remote data monitoring using validated EDC system / software
• Write Monitoring Reports and performing site management, addressing FU activities
• Source Data Verification (SDV / eSDV)
• Check data integrity
• Support the team on the submission of the study to ethics committees / IRBs

Hard & Soft Skills

• Bachelor’s degree / MD or equivalent in technical-scientific field
• Proved experience in clinical monitoring and proven trainings in the field
• Proven GCP-ICH training
• Actual CRA certification as per MoH decree 15 / 11 / 2011
• Fluent in English
• Excellent organizational and time management skills

Additional requirements

• Availability to travel especially in Central-South Italy

What we offer

• Full remote job
• Multicultural, young and dynamic work environment