Italy CRA II - Site Monitoring & Study Oversight

Fortrea; Milano; In loco; EUR 35.000 - 53.000; Tempo pieno

Descrizione del lavoro

Fortrea is seeking an experienced Clinical Research Associate to monitor study sites in Italy, ensuring protocol adherence, patient safety, and regulatory compliance. This role involves pre-study/initiation visits, site management, and collaboration with internal teams to meet timelines.

The successful candidate will have a Master’s in a scientific discipline, hold a CRA certification, and be fluent in Italian and English, with at least two years of monitoring experience.

Competenze

• Master's Degree in a scientific discipline (DM 15/11/2011).
• CRA certification compliant with the Italian Ministerial Decree of 15 November 2011.
• Fluent in Italian and in English, both written and verbal.

Mansioni

• Monitor study sites and ensure regulatory compliance.
• Liaise with vendors and manage travel according to Fortrea policy.
• Prepare accurate and timely trip reports and CRF reviews.
• Ensure data integrity and source documentation review for study data.
• Maintain audit readiness at the site level and adhere to SOPs.

Formazione

Master's Degree in a scientific discipline (DM 15/11/2011)

CRA certification compliant with Italian Ministerial Decree of 15 November 2011

Descrizione del lavoro

Fortrea is seeking an experienced Clinical Research Associate to monitor study sites in Italy, ensuring protocol adherence, patient safety, and regulatory compliance. This role involves pre-study/initiation visits, site management, and collaboration with internal teams to meet timelines.

The successful candidate will have a Master’s in a scientific discipline, hold a CRA certification, and be fluent in Italian and English, with at least two years of monitoring experience.