RWE Delivery Manager - France/Germany

Resilience Care; Toulouse; On-site; EUR 70,000 - 110,000; Full time

Job summary

Resilience Care in France seeks a Lead, Real-World Evidence to drive end-to-end RWE studies across Germany and France. You will own timelines, budgets, site coordination, data quality and sponsor relationships to deliver reliable evidence for oncology/haematology.

Work with Medical, Clinical Operations, Data, Legal, and Quality teams; collaborate with international partners to implement study protocols, GDPR compliance, and AI-assisted data extraction.

Qualifications

• Lead studies end to end with timelines and deliverables.
• Navigate GDPR/DSGVO, ethics, and hospital contracting.
• Oversee CROs and sponsor responsibilities, including pharmacovigilance.
• Track budgets and variances; manage risks and trade-offs.
• Assess clinical data quality and EHR structuring.
• Communicate with German and international stakeholders.

Responsibilities

• Lead studies from contracting to final report, incl. protocol coordination.
• Maintain an actionable project timeline and mitigate risks.
• Track study budgets, site costs and CRO expenses.
• Select and activate sites; coordinate site contracting.
• Be sponsor's operational contact; lead steering committees.
• Collaborate with Medical, Clinical Ops, Data, Legal and Quality.

Skills

Study management

German language

Regulatory knowledge (GDPR/DSGVO)

Budget & cost tracking

Data quality assessment

AI-assisted data extraction

Stakeholder communication

CRO oversight

Ethics submissions

Project coordination

Job description

The Company

Resilience Care, a leading player in remote medical monitoring and a partner in clinical research, is a French company founded in 2021 with a single mission: to provide better care. Our company offers remote monitoring solutions in oncology, gastroenterology, and psychiatry, based on the collection of ePROs combined with AI technologies. These solutions rely on a monitoring platform for healthcare professionals—enabling the early detection of side effects for continuous and proactive care—and a mobile app for patients, empowering them to measure and manage their symptoms using tailored resources. Our solutions optimize patient care, continuously enrich our understanding of patients throughout their healthcare journey, and accelerate clinical research through the collection, structuring, and in-depth analysis of real-world data. Today, our solutions are deployed in routine care for 35,000 patients across more than 200 healthcare facilities, as well as within the framework of around twenty academic and industrial clinical trials. Through this, we put data at the service of healthcare and therapeutic innovation, driven by the ambition to enable every patient to benefit from personalized medicine.

Your Role

In a few words: you will lead the end-to-end delivery of Real-World Evidence (RWE) studies in Germany & France, connecting clinical research, remote monitoring and health data. You will own execution: timelines, budgets, site and partner coordination, deliverable quality and the sponsor relationship.

Your impact

make studies work in practice and generate reliable evidence for oncology and haematology research. The site relationships, methods and tools you build should also make future studies easier to deliver.

Your day to day

• Lead studies from contracting to the final report, including protocol and statistical analysis plan coordination, ethics submissions, data collection and deliverables.


• Maintain an actionable project timeline, anticipate risks and propose solutions before milestones are affected.


• Track study budgets, committed expenditure, site costs and clinical research organisation (CRO) costs.


• Select and activate sites with local teams, coordinate site contracting and oversee CRO partners.


• Act as the sponsor’s primary operational contact and lead steering committees with international pharmaceutical partners.


• Work with Medical, Clinical Operations, Data, Legal and Quality teams, and turn delivery experience into reusable methods.

Your Team

• Your future colleagues: you’ll work closely with Mehdi, Project Manager RWE, on study delivery and shared project-management practices, and with Maxime and Eugénie, Global Pharma Partners, to connect pharmaceutical partners’ needs with practical study execution.


• Your manager: you’ll report to Adil, RWE Lead, who leads Resilience’s Real-World Evidence activities. Adil gives you room to own your projects, with clear priorities and support when decisions need to be made. He values early communication, practical solutions and following through on commitments.


• The little about your team: when the Life Sciences team gets together, Italian food is our go-to, a small tradition we’re happy to share with new colleagues.

Candidate Profile

You are the right person if you know how to

• Lead a clinical or non-interventional study end to end, understanding the dependencies between each stage.


• Navigate the German research environment: ethics committees, GDPR/DSGVO, Länder-level data protection requirements and hospital contracting.


• Oversee a CRO and its deliverables, with a clear understanding of sponsor responsibilities, pharmacovigilance and monitoring plans.


• Track a study budget and make variances, risks and necessary trade-offs visible.


• Assess clinical data quality and discuss electronic health record structuring and AI-assisted extraction.


• Work fluently in German and use professional English in writing and speaking.

You are the right person if you have

• A strong sense of ownership: you follow work through to results rather than stopping at coordination.


• Structured working habits that leave room for anticipation and process improvement.


• The reflex to flag risks early, alongside a proposed course of action.


• Clear communication with scientific, operational and commercial stakeholders.


• Composure when plans change and autonomy in an international, distributed setting.

You are the right person if you have already

• Managed clinical or non-interventional studies with direct responsibility for timelines and deliverables.


• Worked with investigator sites and research partners in the German ecosystem.


• Overseen a CRO from the sponsor side.


• Tracked research project costs and budgets.


• Coordinated cross-functional teams and presented project progress to a sponsor or pharmaceutical partners.

It’s a plus if you have delivered studies in oncology or haematology.

Why join us?

• Contribute to research grounded in real care pathways, working with sites and medical teams.


• Lead studies that combine remote monitoring, patient-reported outcomes and clinical data.


• Own projects end to end, with responsibility for execution and results.


• Build lasting methods and partnerships with an international, multidisciplinary team.