RWE Delivery Manager - French/Germany

Resilience Care; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

Resilience Care is seeking a senior specialist to lead Real-World Evidence studies in Germany and France, overseeing timelines, budgets, sites, CROs, and sponsor relationships. You will ensure study quality and scalable delivery across international collaborations, leveraging remote monitoring, PROs, and clinical data.

You will collaborate with medical, data, legal and QA teams to turn delivery experience into reusable methods, driving efficient study execution in oncology and hematology

Qualifications

• Lead a study end-to-end and understand dependencies between stages.
• Navigate German research environment including ethics, GDPR/DSGVO, and hospital contracting.
• Oversee CROs with sponsor responsibilities, pharmacovigilance and monitoring plans.
• Track study budgets, variances and CRO costs.
• Coordinate cross-functional teams and report progress to sponsors/partners.

Responsibilities

• Lead studies from contracting to final report, including protocol coordination.
• Maintain an actionable project timeline and mitigate risks before milestones.
• Track budgets, site costs and CRO expenditures.
• Select and activate sites with local teams and oversee CRO partners.
• Act as sponsor’s operational contact and lead steering committees with partners.
• Collaborate with Medical, Clinical Operations, Data, Legal and Quality teams to improve methods.

Skills

German fluency

English proficiency

Ownership

Structured work

Risk awareness

Clear communication

Autonomy

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 : to be completed — names, roles and a personal detail they wish to share.




• Your manager : to be completed — name, role, management style and a personal detail to share.




• The little about your team : to be completed — a concrete team strength or anecdote.

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.

Recruitment Process

1. Screening with Elena - 15 min: discuss your motivation and the role’s prerequisites.




2. Manager Fit with Adill - 30min: to dive deeper into your background and product vision




3. Case Study with Adil, Nicoleta and/or Aude and/or Anne-Julie and/or Bertille — Format: a business case sent a few days in advance, followed by a live presentation and Q&A.




4. Team Fit with Mehdi, Eugénie, Ivan, Daniel, Sebastien — 30 min/itw : collaboration fit




5. Strategic Fit with Lucas - 30min

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 [e-mail]

For more information, please check our privacy policy.