Clinical Research Associate (CRA)
The Clinical Research Associate (CRA) role encompasses all activities related to the selection, setup, termination, and archiving of clinical trials.
Key Responsibilities
- Ensure a comprehensive understanding of study protocols, specific requirements, and applicable Standard Operating Procedures (SOPs) throughout the duration of the study.
- Support study team members in the setup, execution, and completion of study activities at both local and central levels.
- Prepare and maintain accurate site-specific study documentation for both site and company/sponsor use, ensuring all documentation is complete, current, accurate, and adequately translated when necessary.
- Conduct site feasibility assessments and perform site visits.
Essential Skills
- Strong self-organization skills.
- Ability to navigate unforeseen situations and manage fluctuating workloads.
- Excellent interpersonal skills with a strong capacity to work collaboratively within a team.
- Proactive approach to identifying and resolving study-related issues.
Requirements
- A degree in a scientific field with a background in clinical research.
- ICH-GCP E6 training certificate.
- CRA certification as per Italian Ministerial Decree (15.11.2011).
- Knowledge of EU/Swiss regulatory requirements is an advantage.
- Previous experience in oncology studies is highly desirable.
- Fluent in English (both spoken and written).
Apply online using the form below. Please note that only applications matching the job profile will be considered.