Director, Quality & Regulatory
Pubblicato il 23-09-2026 - Chiesi in Terni
Overview In this role you steer the global clinical development strategy for key respiratory indications, leading a physician-scientist team across geographies. You will align R&D; and commercial goals, shape trial designs, and drive regulatory success with high scientific and operational impact. You thrive in a cross-functional, matrix environment and help build a high-performing, inclusive culture.
This is a chance to influence patient outcomes at scale within a mission-driven, B Corp-certified company.
Retribuzione / Benefits 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