Clinical Research Associate FREELANCE

Evidilya; Biella; Remoto; EUR 30.000 - 55.000; Tempo pieno

Descrizione del lavoro

A dedicated Contract Research Organization is seeking a Clinical Research Associate to join their Italian team. This full remote position involves conducting study visits, monitoring data integrity, and supporting submissions to ethics committees. Candidates should have a relevant degree, clinical monitoring experience, and be fluent in English. This role offers a dynamic multicultural work environment in a flexible setup.

Servizi

Full remote job

Multicultural, young and dynamic work environment

Competenze

• 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.

Mansioni

• Conduct and perform SQV / Pre-study Visits and monitoring visits.
• Handle remote data monitoring using validated EDC system.
• Write Monitoring Reports and perform site management.

Conoscenze

Clinical monitoring

Fluent in English

Organization

Time management

Formazione

Bachelor’s degree / MD or equivalent in technical-scientific field

Descrizione del lavoro

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

Main 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