Are you an experienced Clinical Research Associate (CRA) based in France with a strong background in medical device studies? We are seeking a dedicated professional to manage clinical monitoring activities across 4-5 investigator sites. This position offers excellent flexibility, requiring an average monthly resource commitment of 50-60% of a full-time role.

As a Clinical Research Associate for this project, you will be responsible for end-to-end site management and clinical monitoring activities. Your core duties will include:

• Comprehensive Site Visits: Planning, conducting, and reporting on Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-out Visits (COV) – executed both on-site and remotely as required.
• Investigator Site Management: Serving as the primary point of contact for 4-5 investigator sites across France, ensuring protocol compliance and seamless communication.
• Stakeholder Communication: Managing direct and transparent communication channels with both the Sponsor and internal teams, including participating in Sponsor training sessions.
• Project Collaboration: Partnering closely with Clinical Trial Leaders via ad-hoc email communication and regular scheduled meetings/telephone calls.

Onboarding & Support: Your integration into the project will be fully managed and overseen by a dedicated CRA Resource Manager, ensuring you have all the tools and training needed to succeed

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