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.Aumenti le sue possibilità di arrivare alla fase del colloquio leggendo la descrizione completa del lavoro e candidandosi tempestivamente.pensionprivate medical insuranceticket restaurantrelocation supportSupport the clinical team in medical and scientific aspects of global clinical studies within the development programContribute to risk/vantaggi assessments of ongoing trials and act as primary medical monitor for assigned studiesContribute to production of regulatory documents (e.G., CTD) and represent the company to authorities and partnersDevelop and enhance management of clinical trials in collaboration with the Clinical Program Leader to ensure validity of design, conduct and interpretationParticipate in program and study teams to support design, conduct,



analysis and data interpretation with timely documentationConduct medical and scientific reviews of trial data with CPL oversightAct as clinical expert in interactions with internal/external stakeholders and maintain knowledge of regulatory and disease-area developmentsInterface with external scientific experts to align on program strategy and patient needsIdentify trends to support internal decision making and ensure timely publication of clinical dataEnsure robust, optimized trial designs and appropriate endpoints, monitoring, and adherence to SOPs and KPIsSupport post-registration xysqume studies to sustain product lifecycle and growth2+ years of experience as Clinical Research Physician/Medical Monitor in pharma or CROsExperience in clinical research in rare diseases or clinical development (trial design, conduct, interpretation)Interpersonal communicationCross-functional collaborationClinical trial design and interpretationRegulatory knowledge (health authorities, guidelines)Medical monitoring and data interpretationClinical Research Physician, Global Rare Diseases milano, lombardia, it#J-18808-Ljbffr

📌 Clinical Research Physician, Global Rare Diseases (Milano)
🏢 Chiesi
📍 Milano