CRA Late Phase Spain

Resourcing Life Science; Gijón; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A global CRO is seeking an experienced Clinical Research Associate for late-phase clinical studies in Spain. The successful candidate will monitor studies, ensuring compliance with GCP and study protocols. This position requires strong background in clinical research and a Bachelor degree in life sciences.

Formación

• Minimum 1 year monitoring experience as CRA within a CRO, Pharma, Biotech.
• Experience with site initiation and close out.
• Experience in commercial studies.

Responsabilidades

• Monitoring clinical studies in phases II-III.
• Assuring adherence to Good Clinical Practices and compliance with all study procedures.
• Supervising study conduct according to GCP requirements.

Conocimientos

Monitoring clinical studies

Good Clinical Practices (GCP)

Investigator integrity

Compliance with study procedures

Educación

Bachelor degree in life-science

Descripción del empleo

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 an experienced Clinical Research Associate Late Phase in Spain.

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
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• FTE : 1.0

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