Clinical Research Physician, Global Rare Diseases
Pubblicato il 15-09-2026 - Chiesi in Lecco
Overview In this role you drive clinical development by supporting global studies and ensuring scientific soundness. You work with cross-functional teams to shape trial design, endpoints and monitoring strategies, while interfacing with health authorities and external experts. You contribute to regulatory documents and publication plans, helping grow our rare-disease therapies. You join a mission-driven company committed to sustainable innovation and patient outcomes.
Retribuzione / Benefits
pension private medical insurance wellbeing programme flexible benefits programme buoni pasto relocation support
Responsabilità
Support the clinical team in medical and scientific aspects of global clinical studies within the development program Contribute to risk/benefit assessments of ongoing trials and act as primary medical monitor for assigned studies Contribute to production of regulatory documents (e.g., CTD) and represent the company to authorities and partners Develop and enhance management of clinical trials in collaboration with the Clinical Program Leader to ensure validity of design, conduct and interpretation Participate in program and study teams to support design, conduct,
analysis and data interpretation with timely documentation Conduct medical and scientific reviews of trial data with CPL oversight Act as clinical expert in interactions with internal/external stakeholders and maintain knowledge of regulatory and disease-area developments Interface with external scientific experts to align on program strategy and patient needs Identify trends to support internal decision making and ensure timely publication of clinical data Ensure robust, optimized trial designs and appropriate endpoints, monitoring, and adherence to SOPs and KPIs Support post-registration studies to sustain product lifecycle and growth
Requisiti fondamentali
Medical Doctor degree 2+ years of experience as Clinical Research Physician/Medical Monitor in pharma or CROs Experience in clinical research in rare diseases or clinical development (trial design, conduct, interpretation) Interpersonal communication Stakeholder management Cross-functional collaboration Clinical trial design and interpretation Regulatory knowledge (health authorities, guidelines) Medical monitoring and data interpretation