This is a fully remote position, open to applicants in Italy.

📋 Description

• Oversee and take responsibility for the advancement of clinical studies at research sites.

• Ensure that clinical trials are carried out, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and all relevant regulations and standards.

• Organize all essential activities needed to establish and oversee a study (e.g., identifying investigators; assisting in the preparation of regulatory submissions, performing pre-study and initiation visits, etc.).

⛳️ Requirements

• A university degree in life sciences, pharmacy, or another health-related field, or equivalent experience in a scientific or healthcare discipline, or be a licensed healthcare professional.

• Minimum of 6 months of experience as a CRA in a CRO or pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies.

• Experience in oncology.

• Possession of CRA Certification.

• Willingness to travel domestically, including overnight stays, potentially committing up to approximately 50-60% of the time to travel.

• Proficiency in both English and Italian.