Medical Affairs Lead

The Company

At Resilience Care, we are transforming cancer care through a clinically validated and reimbursed digital platform dedicated to remote patient monitoring (RPM) in oncology. We operate at the forefront of digital health, integrating AI-enabled predictive approaches to improve patient outcomes, enhance the clinical relevance of care, and generate robust real-world data.

Your Role

In a nutshell: As the Medical Affairs Lead, you will play a central role in shaping and executing our medical and scientific strategy at the intersection of oncology, digital health, and AI-enabled predictive approaches.

This is a strategic and hands‑on role combining medical leadership, evidence generation, scientific engagement, and cross‑functional collaboration. You will act as a key scientific partner, ensuring the clinical integrity of our platform while driving the adoption and understanding of our RPM capabilities across the healthcare ecosystem.

Key Responsibilities

Medical Strategy & Scientific Leadership

• Contribute to the definition, execution, and continuous refinement of Resilience’s medical strategy in oncology and digital health.
• Partner closely with the Senior Director Medical Affairs to shape the scientific vision supporting the development and adoption of Resilience’s RPM and AI-driven capabilities.
• Translate complex clinical, scientific, and technological topics into clear medical positioning and strategic recommendations.
• Identify opportunities to strengthen the clinical relevance, differentiation, and medical value of Resilience’s RPM.
• Contribute to the prioritization of evidence generation initiatives aligned with product, clinical, and business objectives.
• Support the development of scientific narratives and medical communication strategies across stakeholders.

Evidence Generation & Clinical Collaborations

• Lead the scientific evaluation and selection of investigator‑initiated studies (IIS).
• Provide medical support for the execution and follow‑up of clinical collaborations and real‑world evidence (RWE) initiatives.
• Contribute to the design, execution, and follow‑up of clinical projects involving RPM and predictive approaches in oncology.
• Collaborate with clinical, product, and data teams to help define clinically meaningful endpoints and assess the value of predictive models.
• Ensure scientific rigor and operational excellence across all medical activities.

Scientific Engagement & External Medical Relations

• Build and maintain strong relationships with oncologists, academic centers, cooperative groups, and industry partners.
• Represent Resilience in scientific discussions with healthcare professionals, research collaborators, and external stakeholders.
• Contribute to medical education initiatives, scientific exchange activities, and internal training programs.
• Represent the company at congresses, scientific meetings, and public events.
• Support the medical credibility and visibility of Resilience within the oncology and digital health ecosystem.

Publications & Scientific Communication

• Coordinate the preparation and submission of abstracts, posters, manuscripts, and scientific communications.
• Contribute to the development and execution of a coherent publication strategy aligned with corporate and medical priorities.
• Ensure high‑quality scientific outputs and strict compliance with internal SOPs and publication standards.
• Participate in the dissemination of clinical and scientific insights generated through the platform (EDS).

Cross‑functional Collaboration & Medical Impact

• Provide medical and scientific expertise across Product, Clinical, Data Science, Market Access, and Business teams.
• Collaborate with Product and Data teams on the clinical interpretation, relevance, and communication of data generated through the platform, including AI-enabled predictive approaches.
• Help internal teams understand and translate the medical impact and value of clinical and real‑world data generated by Resilience.
• Support selected strategic discussions and customer engagements alongside Business teams, particularly with healthcare institutions, academic centers, and industry partners.
• Operate as a key cross‑functional partner in a fast‑moving and innovation‑driven environment.

Candidate Profile

• Driven by strong scientific rigor combined with a pragmatic, execution‑oriented mindset.
• An excellent communicator, both verbal and written, with the ability to engage scientific, clinical, and cross‑functional stakeholders.
• Genuinely curious about innovation, digital health, data, and AI‑driven healthcare solutions.
• Highly analytical, possessing strong problem‑solving abilities to navigate complex clinical, scientific, and technological topics.
• Familiar with real‑world evidence (RWE) methodologies and healthcare innovation environments.
• Adaptable and comfortable working in a fast‑moving, evolving environment.
• Equipped with an entrepreneurial spirit and a hands‑on “Swiss Army knife” attitude.
• Proactive, demonstrating strong ownership and the ability to turn ideas into tangible impact.

You're the right person if you have already:

• An MD, PharmD, or PhD degree 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, alongside strong scientific writing skills.
• Experience contributing to publication strategies and peer‑reviewed scientific communications.
• Demonstrated ability to collaborate effectively across Medical, Product, Clinical, Regulatory, Data Science, and Business teams.
• Nice to have: Exposure to regulatory and market access frameworks related to digital health and medical devices (e.g., LATM, CE, HTA).

Why join us?

• Direct impact on oncology care: You will play a vital role in transforming the patient journey through clinically validated remote monitoring.
• Pioneering innovation: Work at the cutting edge of science, engaging directly with AI‑driven healthcare solutions and non‑traditional clinical endpoints.
• Strategic cross‑functional exposure: Act as the scientific bridge between Product, Data, and Clinical teams.
• Dynamic scale‑up environment: Combine the scientific rigor of traditional pharma with the agility and digital innovation of a fast‑growing medtech.
• Good to know: This position requires ecosystem engagement, with between 30% and 50% travel time (30% if you are based in Paris).

For more information, please check our privacy policy.