14 set - Como
Chiesi
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
22 set - Lodi
ALI professional
22 set - Genova
Maw - Menwork
22 set - Molfetta
Adecco Italia
22 set - Piemonte
Adecco Talent Attraction