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

📋 Description

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

• Ensure that clinical studies are executed, documented, and reported according to the protocol, standard operating procedures (SOPs), ICH-GCP guidelines, and all relevant regulations and standards.

• Organize all essential tasks needed to initiate and monitor a study, including identifying investigators, assisting in the preparation of regulatory submissions, and performing pre-study and initiation visits.

⛳️ 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.

• A minimum of 6 months experience as a Clinical Research Associate (CRA) within a Contract Research Organization (CRO) or the pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated skills.

• Experience in oncology.

• Possession of CRA Certification.

• Willingness to travel domestically, including overnight stays, with a travel commitment of approximately 50-60%.

• Proficiency in both English and Italian.