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

You're the right person if you are:

• 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).

Recruitment Process

• Screening RH : Interview with Elena the Talent Acqusition Specialist ton asses your motivation (20min)

• Manager Fit : Interview with Aude Guillou the Senior Medical Affairs to assess your scientific vision, medical strategy approach, and oncology expertise (40min)

• Case Study : (30min) Take Home + Debrief with Aude Guillou Senior Director Medical Affairs, Charles Ferté Chief Medical & Patient Officer, Blanche Beneron Chief of Staff to the CMO, Elodie Senior Medical Director, Nicoleta the Director Translational Research.

• Team Fit : Meet the team, Charles Ferté, Nicoleta the Director Translational Research, Elodie Senior Medical Director, Adil Bousfiha + Elena

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 [email protected]

For more information, please check our privacy policy .