1️⃣ What You'll Be Doing

Your job

Job Summary

As a Clinical Operations Manager, you will join a dynamic and fast-growing team at the forefront of digital and patient-centered clinical research. Working closely with the Clinical Operations Lead, you will be directly involved in the execution of high-visibility studies (RIPH2/3, RWE, PSP), 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.

Your daily responsibilities

Clinical Study Oversight

• Coordinate day-to-day operational and logistical activities of clinical studies

• Act as the main point of contact for investigator sites, including oversight of research nurses (IDEs), CRCs, and study-related costs

• Support planning and follow-up of visits (site selection, initiation, monitoring, close-out)

• Actively contribute to study meetings and track key performance indicators

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

Quality & Documentation

• Support the development of tools, trackers, SOPs, and internal templates

• Maintain regulatory documentation (ISF, eTMF) and ensure audit-readiness

• Ensure ongoing compliance with GCP, Jardé Law, ICH guidelines, and GDPR

Cross-functional Collaboration

• Work closely with Medical, Life Sciences, Data, and Product teams

• Contribute to the onboarding and training of field stakeholders (nurses, CRCs, etc.)

• Participate in internal alignment meetings and external study governance committees

• Take part in clinical operations initiatives and cross-functional projects

  This is a field-based role with regular travel expected.

2️⃣ What You'll Bring

You'll definitely have

• A degree in life sciences, pharmacy, clinical research, or biomedical engineering

• 4+ 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 with Anne-Julie Eve, Clinical Operations Lead – Role understanding & motivation

Interview 2 with Grégory Bourdarot, VP Operations – Soft skills

Interview 3 with Anne-Julie Eve – Practical business case & experience deep-dive

Interview 4 with Arlindo Ferreira, Medical Director – Team fit

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

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