Clinical Research Associate

Trovato in: beBee S IT - 4 settimane fa

Lombardia, Italia AL Solutions A tempo pieno

AL Solutions is currently recruiting for a Clinical Research Associate to join their top 5 Global CRO client. As a Clinical Research Associate, you will be responsible for managing and monitoring clinical trials, ensuring adherence to study protocols and regulatory requirements.

You will work closely with study sites, investigators, and sponsors to ensure the successful execution of the trial and the collection of accurate data.

Key Responsibilities:

- Conduct site selection, initiation, monitoring, and close-out visits
- Perform source data verification and review study documents
- Ensure compliance with study protocols, GCP, and applicable regulatory guidelines
- Monitor patient recruitment and retention
- Track and report study progress to project teams

Requirements

Requirements:

- Bachelor's degree in a health-related field or equivalent
- Minimum of 2 years of experience as a Clinical Research Associate
- Knowledge of ICH-GCP guidelines and regulatory requirements
- Excellent communication and organizational skills
- Proficiency in English and Italian
- Availability to travel to study sites in Milan and surrounding areas

Benefits

- Excellent salary and benefits package
- Career development opportunities
- Flexibility with office-based or home-based role
- Encourages work life balance

Whatever your career goals, my client is here to ensure you get there If you are an experienced CRA looking for a new and exciting opportunity with the a lot of room for career progression then please get in touch To apply, please submit your resume at:

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