📝 Your Role

In a few words: You will contribute to the scientific and operational execution of Resilience’s clinical studies, supporting the delivery of key trials — including sponsored studies and upcoming Life Sciences partnerships — with rigor, speed, and compliance. You will work across multiple studies.

How your role contributes to Resilience's success: Resilience is entering a critical phase where delivering high-quality clinical evidence on time is essential to our growth and credibility. By owning end-to-end oversight of our clinical portfolio, you'll ensure that our regulatory deliverables, partner commitments, and scientific outputs are delivered at the required quality level.

What your daily life looks like:

• Clinical Trial Execution (main part): Own scientific and operational oversight of interventional and non-interventional studies—protocol execution, medical monitoring, data integrity, deviation management, reporting, and coordination with Clinical Operations and CROs. You'll move across Resilience study sites (FR, BE, DE) as needed.

• Life Sciences & External Partnerships: Provide scientific and methodological leadership in interactions with pharma partners, including protocol design, feasibility, and evidence positioning.

• Regulatory, GCP & Quality Support: Support regulatory submissions, ensure GCP alignment, participate in audits and readiness activities, and act as a scientific counterpart to QARA when needed.

• Cross-Pathology Clinical Involvement: Engage across Resilience-sponsored studies in multiple therapeutic areas

✨ Your Team

A few members of your team: You'll work closely with Bertille (your manager), Yasmine (QARA Manager), Caroline and Emma (Clinical Scientists), and Elodie (Clinical Development Lead) and Charles (CMO). The team is highly collaborative, with a strong focus on cross-study support and shared ownership.

A few words about your manager: Bertille is the Hiring Manager and Lead Clinical Scientist in oncology at Resilience. She values pragmatism, execution, and collective resilience, and is looking for someone able to operate with autonomy, adapt quickly, and move across studies as priorities evolve. Based in Paris, she recharges in the mountains and loves Lyon's food !

The little ➕ about your team: Even though the team works across different therapeutic areas, members meet regularly to learn from each other and share experience. There is a strong team spirit, with a shared appreciation for outdoor activities and travel, and the team values spending time together beyond day-to-day work.

👤 Candidate Profile

⚙️ You're the right person if you know how to:

• Manage clinical trials end-to-end, from set-up to close-out, including clinical study report and publications

• Apply GCP, regulatory expectations, and data integrity standards in both interventional and real-world studies

• Interact confidently with regulators, investigators, CRO and pharma partners

🙂 You're the right person if you are:

• Pragmatic, execution-oriented, and able to adapt quickly as priorities shift

• Reliable, structured, and comfortable in a high-workload environment

• Team-oriented, with a natural ability to step in, support, and back-up others when needed

• Flexible to move around Resilience sites and to the Paris office

📃 You're the right person if you have already:

• At least 3 years of hands-on experience in clinical research

• Worked in a Pharma, Biotech or Medical Device company

• Formal training in GCP

• PharmD, PhD, or MSc in Life Sciences or equivalent

• French as a working language and good level of English

• Based in metropolitan France

It's a ➕ if you:

• Have experience in oncology or chronic disease research

• Have worked in a scale-up or fast-paced biotech environment
  

💛 Why joining us?

Resilience is on a mission to make healthcare tools accessible to everyone. We're entering a pivotal phase with major clinical trials and Life Sciences partnerships that will shape the future of care delivery. By joining now, you'll be part of a team that's building something impactful, with the opportunity to contribute across multiple studies, work with leading pharma partners, and help shape the clinical strategy of a growing company.

🔄 Recruitment Process

1. Interview 1 – Hiring Manager (Bertille): Assessment of clinical research experience, ability to manage multiple studies, understanding of GCP and compliance, and fit with current operational challenges.

2. Interview 2 – QARA Manager (Yasmine): Regulatory frameworks, experience, knowledge (GCP, etc.).

3. Interview 3 – Day-to-day fit (Caroline or Emma): Team fit, back-ups, fit with other Resilience's chronic diseases scope (transversal work).

4. Interview 4 – Fit & motivation (Elodie): Motivation and knowledge about Resilience company, medical devices / health tech environment, scientific background, global understanding on the field of Oncology, motivations.

5. Interview 5 – CMO (Charles): Final alignment and strategic fit.

6. Interview 6 - Culture fit (Emilie)

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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