Clinical Research Associate II / Senior CRA - Remote

Overview

Rho, an award-winning, stable, full-service CRO known for its collaborative, dynamic culture based in the US, is quickly expanding their presence in Europe. We are a thriving company, and we will deliver global full-service clinical development services and unmatched customer support – worldwide.

Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges.

At Rho, we believe in the power of passionate individuals working together to make a difference in clinical research. As a Clinical Research Associate II / Sr. CRA, you will be a key player in our innovative team, dedicated to ensuring that our clinical trials are conducted with the utmost integrity and quality. Your expertise will help us navigate the complexities of clinical research as we strive to deliver meaningful solutions to healthcare challenges.

The Clinical Monitoring team at Rho is known for its collaborative spirit and commitment to excellence. Join us to not only advance your career but also contribute to a culture that celebrates innovation, supports professional growth, and values every team member's input.

This is a permanent CRA II / Senior CRA role to be home based role in Italy.

In Short

• Conduct clinical monitoring visits and ensure compliance with GCP and protocol.
• Document observations and maintain study documentation.
• Assist in site feasibility assessments and vendor selection.
• Mentor junior CRAs and support training initiatives.
• Participate in the preparation of documents for Ethics Committee submissions.
• Verify handling of investigational products at sites.
• Support payment processes and data review for invoicing.
• Engage in risk assessment and action for adverse events.
• Contribute to the development of study tools and materials.
• Collaborate with clinical team leads on project management tasks.

Requirements

• Experience in clinical research monitoring.
• Knowledge of Good Clinical Practice (GCP).
• Strong documentation and communication skills.
• Ability to mentor and train junior staff.
• Experience with site feasibility and vendor assessments.
• Familiarity with regulatory submission processes.
• Proficient in handling investigational medicinal products.
• Strong analytical skills for data review.
• Ability to work independently and as part of a team.
• Detail-oriented with strong organizational skills.

Benefits

• Competitive salary and benefits package.
• Opportunities for professional growth and development.
• Collaborative and dynamic work environment.
• Flexible work arrangements including remote work.
• Supportive team culture that values input from all members.