Medical Science Liaison - Medical affairs
France - Remote
📝 Your Role
In a few words:
At Resilience, we are transforming cancer care through a clinically validated, reimbursed digital platform for remote patient monitoring. As Medical Affairs Lead, you will serve as the scientific and clinical backbone of our commercial and research strategy. This is a highly cross-functional role, combining clinical leadership, real-world evidence generation, and strategic support to internal teams and external partners. You will be instrumental in reinforcing the medical credibility of our platform, supporting our growth across hospitals, biopharma sponsors, and new therapeutic areas.
What your day-to-day looks like:
1. Medical Engagement & Scientific Leadership to support Commercial and Operational efforts
Act as the primary medical partner for Sales, and Life Sciences teams.
Represent Resilience in customer meetings, especially academic centers and industry sponsors.
Support the integration of Resilience into clinical trials (early development, pivotal, RWE).
Lead internal training initiatives and help shape our scientific storytelling.
Represent Resilience at congresses, public events, and in conversations with key stakeholders.
2. Evidence Generation & Real-World Data
Lead the execution and follow-up of investigator-led studies, clinical collaborations.
Ensure Resilience is included in clinical trials, local projects, and external partnerships, reinforcing the scientific credibility of the platform.
3. Publication & Scientific Communication
Coordinate and ensure high-quality, timely submissions of abstracts, posters, and peer-reviewed publications.
Develop and maintain a cohesive medical publication strategy.
Ensure compliance with internal SOPs and medical communication standards.
4. Sales & Strategic Support
Provide cross-functional medical expertise to Product, Regulatory, Legal, and Market Access.
Guide clinical prioritization of features and contribute to scientific development roadmaps.
Contribute to the preparation of regulatory and funding dossiers (e.g., LATM, Bpifrance).
⚙️ You’re the right person if you have:
Familiarity with regulatory processes (LATM, CE, HTA) and RWE methodologies.
Publication strategy and experience with peer-reviewed scientific communication.
🙂 You’re the right person if you have :
Cross-functional collaboration
Adaptability and problem-solving mindset
Excellent communication, both verbal and written
Entrepreneurial spirit and “Swiss Army knife” attitude
Scientific rigor paired with operational execution
Excellent communication skills
📃 You’re the right person if you have already:
MD, PharmD, or PhD with strong knowledge of clinical research and oncology.
At least 5 years of experience in Medical Affairs in pharma, biotech, or medtech.
Fluency in English and French, with strong scientific writing skills.
💛 Resilience is the company for you if you:
Want to join an ambitious and meaningful project
Enjoy working on a variety of topics
Want to help grow a dynamic young company
3️⃣ Recruitment Process
Interview 1 with Charles, our Chief Medical Officer and Alex, one of our Medical Director – Screening
Interview 2 with Carlota, our Medical chief of staff
Interview 3 with Sébastien Richard, our Sales Country Manager France
Interview 4 with Emilie, our HRBP - Culture fit
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.
ApplyJob Profile
RestrictionsFully remote in France
Tasks- Coordinate scientific publications
- Develop scientific storytelling
- Lead evidence generation and collaborations
- Provide medical expertise to teams
- Represent company at events
- Support clinical and commercial efforts
- Support regulatory and funding dossiers
- Train internal teams
BioTech CE Certification Clinical Leadership Clinical trial support Cross-functional Collaboration English Language French Language Hta LATM Medical Affairs Medical Engagement Medtech Oncology Operational Execution Peer-Reviewed Scientific Communication Pharma Pharmacology Publication strategy Real-World Evidence Generation Regulatory processes RWE Methodologies Scientific communication Scientific Writing
Experience5 years
Education Timezones