RWE Delivery Manager – French/Germany

Job not on LinkedIn

🔥 0 minutes ago

🌐 France, Germany – Remote

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⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 Ghost score 10%

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🗣️🇩🇪 German Required

🗣️🇫🇷 French Required

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Logo of Resilience

Resilience

1001 - 5000 employees

Founded 2020

🏭 Manufacturing

🏥 Healthcare

📦 Logistics

Manufacturing • Healthcare • Logistics

Resilience is a leading biomanufacturing innovation company focused on the development of novel medicines. Specializing in the manufacturing of complex medicines such as cell and gene therapies, Resilience partners with small and mid-sized biotech firms to provide customized solutions that leverage cutting-edge technologies and scientific advancement. Their approach includes high-tech, end-to-end drug substance and drug product manufacturing capabilities aimed at ensuring rapid, safe, and scalable production. Resilience operates primarily in North America, with expertise in delivering regulatory-compliant solutions across global markets, enhancing the reliability and accessibility of biopharmaceutical supply chains.

📋 Description

• Lead Real-World Evidence studies from contracting through final report • Coordinate protocols, statistical analysis plans, ethics submissions, data collection and deliverables • Maintain project timelines, anticipate risks and propose mitigations • Track study budgets, committed expenditure, site costs and CRO costs • Select and activate sites with local teams • Coordinate site contracting and oversee CRO partners • Serve as the sponsor’s primary operational contact • Lead steering committees with international pharmaceutical partners • Collaborate with Medical, Clinical Operations, Data, Legal and Quality teams • Develop reusable methods from delivery experience

🎯 Requirements

• Experience leading clinical or non-interventional studies end to end • Knowledge of the German research environment, including ethics committees, GDPR/DSGVO, Länder-level data protection requirements and hospital contracting • Experience overseeing a CRO and its deliverables from the sponsor side • Understanding of sponsor responsibilities, pharmacovigilance and monitoring plans • Experience tracking study budgets, committed expenditure, site costs and CRO costs • Ability to assess clinical data quality and discuss electronic health record structuring and AI-assisted extraction • Fluency in German • Professional English proficiency in writing and speaking • Experience working with investigator sites and research partners in the German ecosystem • Experience coordinating cross-functional teams and presenting project progress to sponsors or pharmaceutical partners • Experience in oncology or haematology is a plus

🏖️ Benefits

• Contribute to research grounded in real care pathways, working with sites and medical teams • Lead studies combining remote monitoring, patient-reported outcomes and clinical data • End-to-end project ownership with responsibility for execution and results • Opportunity to build lasting methods and partnerships with an international, multidisciplinary team

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