ClinicalResearchAssociate

1️⃣ WHAT YOU'LL BE DOING 📝 Your job In a few words As a Clinical Research Associate (CRA) at Resilience under a 1-year fixed-term contract (CDD), you will join a committed, fast-growing, and agile team at the forefront of digital, patient-centered clinical research. You will be directly involved in monitoring and managing ambitious multicenter studies across several therapeutic areas. You will play a key role in ensuring quality and compliance at every stage of clinical execution. This is a hands-on role offering strong exposure, autonomy, and the opportunity to grow within a collaborative and impact-driven environment. Your day-to-day responsibilities - Conduct site monitoring visits (initiation, routine, close-out) according to study plans - Ensure quality and completeness of clinical data and eCRFs - Protocol deviation tracking & CAPA management - eTMF completeness ownership - Monitor recruitment metrics and oversee timely query resolution - Serve as the key operational contact for investigator sites - Site feasibility & qualification contribution - Support visit planning and coordination with internal teams and vendors - Actively participate in study meetings and follow-up actions - Help implement tracking tools, dashboards, and internal process documentation - Contribute to continuous improvement efforts and share operational insights with the team 2️⃣ What You'll Bring ⚙️ You definitely have - A scientific or paramedical degree (Bachelor’s, Master’s, DU FIEC or equivalent) - A CRA or Clinical Research certification - A first experience or strong internship in clinical research - A good knowledge of ICH-GCP and clinical site operations - Fluency in French and English (oral and written) - A valid driving license and willingness to travel (~40% of your time across France and Europe 🙂 You’re the right person if you - Are rigorous, organized, and proactive - Communicate clearly and build strong professional relationships - Know how to manage multiple priorities a