ppIn 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. /pullipension /liliprivate medical insurance /liliticket restaurant /lilirelocation support /liliSupport the clinical team in medical and scientific aspects of global clinical studies within the development program /liliContribute to risk/vantaggi assessments of ongoing trials and act as primary medical monitor for assigned studies /liliContribute to production of regulatory documents (e.g., CTD) and represent the company to authorities and partners /liliDevelop and enhance management of clinical trials in collaboration with the Clinical Program Leader to ensure validity of design, conduct and interpretation /liliParticipate in program and study teams to support design, conduct,



analysis and data interpretation with timely documentation /liliConduct medical and scientific reviews of trial data with CPL oversight /liliAct as clinical expert in interactions with internal/external stakeholders and maintain knowledge of regulatory and disease-area developments /liliInterface with external scientific experts to align on program strategy and patient needs /liliIdentify trends to support internal decision making and ensure timely publication of clinical data /liliEnsure robust, optimized trial designs and appropriate endpoints, monitoring, and adherence to SOPs and KPIs /liliSupport post-registration studies to sustain product lifecycle and growth /lili2+ years of experience as Clinical Research Physician/Medical Monitor in pharma or CROs /liliExperience in clinical research in rare diseases or clinical development (trial design, conduct, interpretation) /liliInterpersonal communication /liliCross-functional collaboration /liliClinical trial design and interpretation /li liRegulatory knowledge (health authorities, guidelines) /li liMedical monitoring and data interpretation /li /ulpClinical Research Physician, Global Rare Diseases treviso, veneto, it /p /p #J-18808-Ljbffr

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