Clinical Research Associate – France

Resourcing Life Science; France; Sur place; EUR 42 000 - 54 000; Plein temps

Résumé du poste

Resourcing Life Science is seeking a Clinical Research Associate (CRA) in France to monitor clinical studies in phases II-III and ensure compliance with GCP and study procedures. You will identify, qualify and initiate investigators and sites, and supervise conduct according to regulations.

The role requires a life-science degree, 1+ year CRA monitoring experience in France, and fluency in English and French, along with excellent communication and a valid driving license.

Qualifications

• Bachelor degree in life-science or equivalent.
• Minimum 1 year monitoring experience as CRA in a CRO, Pharma or Biotech in France.
• Experience in clinical studies phase II-III.
• Experience with site initiation and close-out.
• Experience with commercial studies.
• Full-time position (FTE 1.0).
• Fluent English and French.

Responsabilités

• 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.

Connaissances

Fluent English

Fluent French

Excellent communication skills

Valid driver’s license

Formation

Bachelor degree in life-science

Description du poste

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 in France

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 France
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• Fluent English & French
• Excellent communication skills
• A full clean drivers license
• FTE: 1.0