CRA Italy – Regional Monitoring

Resourcing Life Science; Italia; In loco; EUR 30.000 - 45.000; Tempo pieno

Descrizione del lavoro

A global CRO provider is seeking a Clinical Research Associate to conduct regional monitoring in Italy. The role requires monitoring clinical studies in phases II-III and ensuring compliance with Good Clinical Practices. Candidates must have a Bachelor degree in life-science, a minimum of one year of monitoring experience in a CRO, Pharma, or Biotech, and be fluent in both English and Italian. A clean driver's license is also required. This role offers the opportunity to work at the forefront of clinical research.

Competenze

• Minimum 1 year monitoring experience as CRA within a CRO, Pharma, or Biotech in Italy.
• Experience in commercial studies.
• Experience with site initiation and site close out.
• Experience in clinical studies phase II-III.

Mansioni

• Monitoring clinical studies in phases II-III.
• Assuring adherence to Good Clinical Practices and compliance with all study procedures.
• Identification, qualification, and initiation of investigators and their sites.
• Supervising study conduct according to GCP requirements.

Conoscenze

Fluent English

Fluent Italian

Excellent communication skills

Formazione

Bachelor degree in life-science

Descrizione del lavoro

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate Regional Monitoring in Italy

Job Overview

• Monitoring clinical studies in phases II-III
• Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
• Identification, qualification and initiation of investigators and their sites.
• Supervising study conduct according to GCP requirements and all applicable laws.

Key Requirements

• Bachelor degree in life-science
• Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Italy
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• Fluent English & Italian
• Excellent communication skills
• A full clean drivers license
• FTE: 1.0

If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or email [e-mail]