Clinical Research Associate II – Italy (Home-Based)

Linical; Milano; Ibrido; EUR 45.000 - 65.000; Tempo pieno

Vantaggi offerti da questo lavoro

Home-based flexibility

International trials

Team environment

Competitive package

Descrizione del lavoro

Linical Milano (Italy) is seeking a Clinical Research Associate II to oversee multiple investigative sites across Italy. This on-site role requires ensuring trials are conducted per study protocols, ICH-GCP, and regulatory standards, with significant travel and site management responsibilities.

The successful candidate will have a Life Sciences degree with CRA training, at least 4 years in clinical research and 2 years monitoring experience, and fluency in Italian with English proficiency.

Competenze

• Life Sciences degree or equivalent with recognised CRA training.
• Minimum 4 years' clinical research experience.
• Minimum 2 years' monitoring experience as a CRA.
• Strong knowledge of ICH-GCP, trial regulations, and site management.

Mansioni

• Conduct site qualification, initiation, monitoring and close-out visits.
• Ensure patient safety, data integrity and protocol compliance.
• Perform source data verification and review documentation.
• Manage site relationships and provide ongoing investigator support.
• Assist with ethics committee and regulatory submissions as required.
• Monitor investigational product accountability and site performance.
• Maintain Trial Master File (TMF) documentation and assist with queries.
• Collaborate with cross-functional study teams to deliver trials.

Conoscenze

Communication skills

Organisational skills

Problem-solving

Italian language

English language

Independent working

Travel readiness

Formazione

Life Sciences degree

CRA training

Descrizione del lavoro

Linical Milano (Italy) is seeking a Clinical Research Associate II to oversee multiple investigative sites across Italy. This on-site role requires ensuring trials are conducted per study protocols, ICH-GCP, and regulatory standards, with significant travel and site management responsibilities.

The successful candidate will have a Life Sciences degree with CRA training, at least 4 years in clinical research and 2 years monitoring experience, and fluency in Italian with English proficiency.