Clinical Research Associate

Resilience Care; Paris; Sur place; EUR 35 000 - 45 000; Plein temps

Résumé du poste

A digital health company in France is seeking a Clinical Research Associate to support multicenter studies. Responsibilities include site monitoring visits, ensuring data quality, and overseeing operational processes. The ideal candidate holds a scientific or paramedical degree, has experience in clinical research, and is fluent in French and English. This is a field-based position with the opportunity for growth.

Qualifications

• First experience or strong internship in clinical research.
• Rigorous, organized, and proactive.

Responsabilités

• Conduct site monitoring visits according to study plans.
• Ensure quality and completeness of clinical data.
• Monitor recruitment metrics and oversee timely query resolution.

Connaissances

Fluency in French and English

Knowledge of ICH-GCP

Organizational skills

Proactivity

Communication skills

Formation

Scientific or paramedical degree

Description du poste

Overview

As a Clinical Research Associate (CRA) at Resilience, 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. This is a field-based position with regular travel.

What you\'ll be doing

• Conduct site monitoring visits (initiation, routine, close-out) according to study plans
• Ensure quality and completeness of clinical data and eCRFs
• Monitor recruitment metrics and oversee timely query resolution
• Serve as the key operational contact for investigator sites
• 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
• Support the development of internal processes and contribute to cross-functional initiatives led by Clinical Operations team

What you\'ll bring

• A scientific or paramedical degree (Bachelor’s, Master’s, DU FIEC or equivalent)
• 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)

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

Recruitment

Interview 1 with Anne-Julie Eve, Clinical Operations Lead – Introduction and motivation

Interview 2 with Grégory Bourdarot, VP Operations – Soft skills

Interview 3 with Emilie Filoni – Culture fit

Start date : as soon as possible

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 [e-mail]

For more information, please check our privacy policy.