Chloe O'Shea is proud to partner with a leading global CRO providing innovative clinical trial solutions. We are seeking an experienced Clinical Research Associate (CRA) to join a dedicated team based in France for a single-sponsor opportunity in CNS. This role offers a manageable workload of 5-8 site visits per month, allowing you to focus on high-quality monitoring and site management.
The Role
As a Clinical Research Associate (CRA), you will play a key role in driving the success of clinical trials across France. Collaborating with the sponsor and investigative sites, you will ensure compliance with protocols, GCP guidelines, and regulatory requirements. With a focus on building strong site relationships, this position is ideal for professionals passionate about advancing clinical research in a supportive and innovative environment.
Key Responsibilities
* Perform site qualification, initiation, routine monitoring, and close-out visits across France.
* Ensure clinical sites adhere to ICH-GCP guidelines, applicable regulations, and protocol-specific requirements.
* Verify the accuracy and integrity of clinical data and oversee the management of investigational products (IP).
* Identify, resolve, and escalate site-related issues to ensure timely and efficient trial progress.
* Foster and maintain strong professional relationships with site staff and sponsor representatives.
* Provide training and guidance to site staff to ensure protocol compliance and study quality.
* Maintain essential trial documentation and update systems such as CTMS, eTMF, and EDC.
Requirements
* A Bachelor’s degree in a health or life sciences discipline.
* At least 3 years of independent monitoring experience as a CRA
* Strong knowledge of ICH-GCP guidelines and French regulatory requirements.
* Experience in conducting site visits and monitoring activities across multiple therapeutic areas.
* Fluent in French and English, both written and spoken.
* Strong organizational skills and ability to manage priorities effectively.
What’s in It for You?
* Competitive salary with additional benefits.
* Opportunities for career growth within a global organization.
* Flexible working environment with manageable travel requirements.
* Exposure to innovative technologies and methodologies in clinical research.
* Comprehensive health benefits and wellness programs.
If you are a motivated professional looking to advance your career as a Clinical Research Associate, we would love to hear from you. Apply now and join a team dedicated to driving innovation in clinical trials!
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