Clinical Research Associate - Italy

Posted 06 January 2023
Job type Permanent
Contact NameValerie Kalna

Job description



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.



Phone:  0203 892 8777