Clinical Research Associate

About the Role

IQVIA is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their team in Modena, Italy. This is a permanent, onsite position focused on ensuring the successful execution of clinical studies.

Key Responsibilities

As a Clinical Research Associate, you will be responsible for:

• Performing site monitoring visits, including site selection, initiation, routine monitoring, and close-out visits.
• Ensuring that clinical sites adhere to study protocols, applicable regulations, and guidelines.
• Verifying that study data is reported accurately and in accordance with sponsor requirements.
• Conducting monitoring activities in compliance with the contracted scope of work and regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Managing and overseeing clinical trial sites to ensure smooth study operations.

Requirements

• Proven experience in Clinical Research.
• Strong understanding of Site Management principles.
• Knowledge of Good Clinical Practice (GCP) and regulatory requirements.
• Experience in clinical trial monitoring.
• Familiarity with regulatory requirements in the healthcare industry.

About IQVIA

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to driving innovation and improving patient outcomes worldwide.