Your Role

In a few words: You will contribute to the scientific and operational execution of Resiliences 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 Resiliences 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 youll 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 studiesprotocol execution medical monitoring data integrity deviation management reporting and coordination with Clinical Operations and CROs. Youll 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: Youll 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 Lyons 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

Youre 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

Youre 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

Youre 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

Its 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. Were entering a pivotal phase with major clinical trials and Life Sciences partnerships that will shape the future of care delivery. By joining now youll be part of a team thats 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 Resiliences 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

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Required Experience:

IC