RWE Delivery Manager – French/Germany

• 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

• 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

• 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