Oncology CRA — Site Monitoring & Study Execution

BeiGene, Ltd.; Milano; Ibrido; EUR 45.000 - 56.000; Tempo pieno

Descrizione del lavoro

BeOne is seeking a Clinical Research Associate in Milan to perform site monitoring in oncology/hematology trials, ensure compliance with ICH-GCP and local regulations, and support study startup and regulatory submissions.

The successful candidate will collaborate with the Regional Clinical Operations Manager, conduct visits, generate monitoring reports, and help achieve study milestones while maintaining data quality.

Competenze

• BS in a relevant scientific discipline and minimum of 2 years of monitoring experience.
• Experience in oncology/hematology trials preferred.
• Fluent in English and Italian (writing and speaking).

Mansioni

• Perform feasibility, site identification, selection and evaluation.
• Conduct monitoring visits (pre-study, initiation, routine, closeout).
• Prepare monitoring visit reports in line with ICH-GCP and SOPs.
• Track site regulatory submissions, recruitment, CRF completion and data queries.
• Ensure inspection readiness and support study milestones.

Conoscenze

English proficiency

Italian proficiency

Formazione

Bachelor's degree in a relevant scientific discipline

Strumenti

MS Word

Excel

MS Project

PowerPoint

Outlook

Descrizione del lavoro

BeOne is seeking a Clinical Research Associate in Milan to perform site monitoring in oncology/hematology trials, ensure compliance with ICH-GCP and local regulations, and support study startup and regulatory submissions.

The successful candidate will collaborate with the Regional Clinical Operations Manager, conduct visits, generate monitoring reports, and help achieve study milestones while maintaining data quality.