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 at once

• Want to grow your expertise while working on innovative, high-impact clinical studies

• Thrive in agile and collaborative environments

• Are genuinely excited about digital products and AI-powered tools

3️⃣ Recruitment

Interview 1 with Elena (20min)

Interview 2 with Anne-Julie Eve, Clinical Operations Lead – Introduction and motivation (30min)

Interview 3 - Case Study with Anne-Julie, Agathe Combes, Ayelen Gallardo (45min)

Interview 4 with Blanche Berneron

GDPR : Your personal data will be processed for the purposes of recruitment related activities, which include setting up and conducting interviews and tests for applicants, evaluating and assessing the results thereto, and as is otherwise needed in the recruitment and hiring processes. They will be available only for people involved in the process and erased after 2 years of inactivity.

Under GDPR and as Resilience attach great importance to privacy, please note that you have the right to request access to your personal data, to request that your personal data be rectified or erased. The Data Protection Officer can be contacted at [email protected]

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