Senior Director, Clinical Excellence AIR
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* flexible working
* remote working
* relocation support
* tax assistance for foreign colleagues
* people-care services
* commitment to wellbeing Responsabilità
* Define and drive the clinical development strategy for Bronchiectasis, Pulmonary Hypertension and Interstitial Lung Diseases in line with R&D and commercial objectives
* Serve as senior clinical representative in global cross-functional governance for asset development and prioritization
* Maintain in-depth knowledge of scientific, regulatory, and competitive landscapes within respiratory medicine
* Lead, develop, and inspire a team of Clinical Development professionals across multiple geographies
* Establish clear goals, performance expectations, and development plans for individuals and the team
* Foster a culture of trust, empowerment, collaboration, and accountability
* Drive operational excellence through coaching, resource planning, and risk mitigation
* Participate in departmental and broader talent development, succession planning, and leadership forums
* Provide medical and scientific leadership across all phases of clinical trials
* Ensure optimal study designs, endpoints, and execution strategies to support regulatory approval and market access
* Contribute to health authority briefing documents and major regulatory submissions Requisiti fondamentali
* Minimum 8–10 years in pharmaceutical R&D with substantial clinical development leadership roles
* Significant experience designing and executing comprehensive clinical development plans
* Track record of driving programs from early development to regulatory submission and approval
* Experience leading global clinical teams in matrixed environments
* MD with board certification in pulmonology or relevant area preferred
* English fluency
* Strong leadership presence
* Strategic thinking
* Exceptional communication and influencing at senior levels
* Data interrogation and interpretation to optimize clinical/scientific/business decisions
* Strategic planning and program management
* Regulatory submission experience
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