Oncology Clinical Research Associate – Hybrid/Remote

IQVIA; Paris; Hybride; EUR 55 000 - 85 000; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Monitoring professional to conduct site visits in accordance with the study protocol, GCP and regulatory requirements. You will coordinate with experienced staff and manage monitoring activities across assigned sites.

Responsibilities include training site staff, maintaining TMF and ISF, tracking regulatory submissions, recruitment and data queries, and travel nationwide. Hybrid or home-based work is available in Paris, Lyon, Marseille.

Qualifications

• Bachelor's Degree in scientific discipline or healthcare preferred; equivalent experience acceptable.
• 2 years clinical oncology experience mandatory.
• Proficiency in Microsoft Word, Excel and PowerPoint.
• Excellent written and verbal English communication.
• Ability to travel nationwide and work in hybrid/home-based settings in France.

Responsabilités

• Perform site monitoring visits (selection, initiation, monitoring and close out) per scope and GCP/ICH.
• Administer protocol and study training to sites and maintain regular communication.
• Ensure quality and integrity of site practices and manage regulatory submissions, recruitment and CRF data tasks.
• Verify TMF and ISF documentation in compliance with GCP/ICH and local regulations.
• Create site visit reports and follow-up letters; collaborate with study team.

Connaissances

Clinical monitoring

Regulatory knowledge

Communication skills

Team collaboration

Time management

Formation

Bachelor's degree in life sciences/healthcare

Equivalent combination of education and experience

Outils

Microsoft Word

Microsoft Excel

PowerPoint

Description du poste

IQVIA is seeking a Clinical Monitoring professional to conduct site visits in accordance with the study protocol, GCP and regulatory requirements. You will coordinate with experienced staff and manage monitoring activities across assigned sites.

Responsibilities include training site staff, maintaining TMF and ISF, tracking regulatory submissions, recruitment and data queries, and travel nationwide. Hybrid or home-based work is available in Paris, Lyon, Marseille.