Clinical Trial Manager

1️⃣ What You'll Be Doing Your job Job Summary As a Clinical Trial Manager (CTM), you will join a dynamic and fast-growing team at the forefront of digital and patient-centered clinical research. Reporting to a Clinical Operations Lead (COPL), you will you will ensure the flawless execution of a diverse portfolio including Resilience-sponsored and ISR, across several therapeutic areas. This is a rare opportunity to consolidate your on-the-ground expertise while stepping into broader coordination missions: stakeholder management, process structuring, regulatory submissions, and contractual follow-up. You’ll be working in a rigorous yet supportive environment, designed for agility, innovation, and impact. Regular travel expected. Your daily responsibilities Clinical Study Oversight - Coordinate day-to-day operational and logistical activities of clinical studies - Support planning and follow-up of visits (site selection, initiation, monitoring, close-out) - Actively contribute to study meetings and track key performance indicators - Oversee study delivery at site, ensuring quality and client satisfaction. Regulatory & Contractual Coordination - Assist with regulatory submissions (ethics committees, ANSM) - Monitor contractual workflows: single-site agreements, amendments, budget annexes - Liaise with legal, clinical, and institutional stakeholders to ensure compliance - Contribute to site budget tracking and payment follow-up in coordination with Finance Quality & Documentation - Support the development of tools, trackers, SOPs, and internal templates - Maintain regulatory documentation and ensure audit-readiness - Ensure ongoing compliance with GCP, Jardé Law, ICH guidelines, and GDPR Cross-functional collaboration - Work closely with Clinical Scientists, Biostatistics, and Product teams - Participate in internal alignment meetings and external study governance committees - Take part in clinical operations initiatives and cross-functional projects 2️⃣ What You'll Bring You'll definitely have - A degree in life sciences, pharmacy, clinical research, or biomedical engineering - 2+ years of experience in clinical research (CRA, site manager, or junior project management) - Professional fluency in both French and English, written and spoken You’re the right person if you - Are structured, rigorous, and autonomous with strong prioritization skills - Thrive in fast-moving, cross-functional environments - Are curious, resourceful, and an excellent communicator - Want to grow in an environment where ownership, impact, and collaboration are key 3️⃣ Recruitment Interview 1 (Role understanding & motivation) with Anne-Julie Eve, Clinical Operations Lead or Agathe Combes - Clinical Operations Lead Interview 2 (Clinical Scientist fit) with Bertille Pommier, or Emma Touré Cuq Clinical Scientist Interview 3 (Practical business case & experience deep-dive) with Anne-Julie Eve Interview 4 (Medic vision & Soft skills) with Charles Ferté, CMO Interview 5 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 privacy@resilience.care For more information, please check our privacy policy https://patients.resilience.care/politique-de-confidentialite.