Clinical Research Associate FREELANCE

Evidilya; Modena; Remoto; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A multinational research organization is seeking a Clinical Research Associate to support its operational team in Italy. Key responsibilities include conducting monitoring visits, handling data monitoring, and supporting submissions to ethics committees. Ideal candidates should have a degree in a technical-scientific field, experience in clinical monitoring, and fluent English skills. Full remote work opportunity is available within a dynamic work environment.

Servizi

Full remote work opportunity

Multicultural work environment

Competenze

• Proven experience in clinical monitoring and relevant training.
• GCP-ICH training certification.
• Current CRA certification per MoH decree 15/11/2011.
• Availability to travel, especially in Central-South Italy.

Mansioni

• Conduct SQV / Pre-study Visits and monitoring visits.
• Handle remote data monitoring using validated EDC system.
• Write Monitoring Reports and perform site management.
• Perform Source Data Verification (SDV / eSDV).
• Support the submission to ethics committees / IRBs.

Conoscenze

Clinical monitoring

Organizational skills

Time management

Fluent in English

Formazione

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

Strumenti

EDC system/software

Descrizione del lavoro

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. We are 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 perform site management, including follow-up activities
• Perform Source Data Verification (SDV / eSDV)
• Check data integrity
• Support the team in the submission of the study to ethics committees / IRBs

Hard & Soft Skills :

• Bachelor’s degree / MD or equivalent in a technical-scientific field
• Proven experience in clinical monitoring and relevant training in the field
• Proven GCP-ICH training
• Current 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 work opportunity
• Multicultural, young, and dynamic work environment