Clinical Research Associate II - Remote

Overview

Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA II) to join our A-team. As a CRA II at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

In Short

• Independently manage all aspects of monitoring for assigned clinical trials.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
• Build strong site relationships, acting as a primary point of contact.
• Identify and resolve site issues, escalating as needed.
• Mentor and support junior CRAs, sharing knowledge and best practices.
• Travel throughout Italy for site visits.
• Contribute to the success of clinical trials.
• Work collaboratively with a team to ensure high-quality data collection.
• Act as a bridge between sponsor and site.
• Support trial integrity and patient safety.

Requirements

• Experience as a Clinical Research Associate.
• Strong understanding of clinical trial processes.
• Ability to travel for site visits.
• Excellent communication skills.
• Proven ability to mentor team members.

Benefits

• Opportunity to work in a collaborative environment.
• Support for professional growth and development.
• Contribute to impactful clinical trials.
• Work with a dedicated team.
• Flexible work culture.