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.

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pension private medical insurance buoni pasto relocation support

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 xysqume studies to sustain product lifecycle and growth

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

Cross-functional collaboration

Clinical trial design and interpretation

Regulatory knowledge (health authorities, guidelines)

Medical monitoring and data interpretation

Clinical Research Physician, Global Rare Diseases ancona, marche, it

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