CRA - REDUCED TRAVEL

Position Summary

Our award-winning CRO client are actively recruiting for a Clinical Research Associate (I-III) into their operations team.

The role is full-time, permanent and fully remote in Italy with reduced travel requirements.

This is a fantastic opportunity for an experienced CRA to continue their passion within clinical monitoring across 1 or 2 protocols. You will be responsible for site management for 2/3 sponsors with the CROs SOPs. The studies are in phases II-IIIb and will be across multiple therapeutic areas.

You will be responsible for:

• Management of sites for assigned studies, with responsibility for the successful management of the site through to close-out, in accordance with the clinical monitoring plan.
• Developing relationships with investigator site staff to ensure that clinical metrics are met.
• Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and working diligently to relevant guidelines.

You will bring:

• Life Science degree
• Experience as a monitor/CRA - 18 months +
• Certification to monitor in Italy
• Fluent in Italian and English
• Experience in the oversight of phases II-III of the clinical trial process
• Site organization and communication
• Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
• Knowledge of ICH-GCP guidelines and local and international regulatory requirements

If you don’t want to miss out on this opportunity, please get in touch ASAP.

Email: Valerie.kalna@biotalent.com

Phone:  0203 892 8777