Experteer Overview In this role you will support the design, execution and analysis of oncology and rheumatology clinical trials, reporting to the Chief Medical Officer. You will guide trial design, monitor efficacy and safety trends, and review regulatory and pharmacovigilance documents. You will interact with principal investigators and site staff, contribute to scientific publications and conferences, and work closely with cross‐functional teams to advance Philogen's development programs. This position offers a hands‐on opportunity to shape trial performance and scientific communication in a fast‐paced biotech environment. Retribuzione / Benefits Contribute to design,



execution and analysis of clinical trials in oncology and rheumatology Provide expert guidance in designing and writing clinical trials Support monitoring of efficacy and safety by reviewing data and feeding analysis datasets Review regulatory and pharmacovigilance documentation Interact with Principal Investigators and clinical site staff to advance trials Disseminate scientific knowledge through publications and conferences Collaborate with cross‐functional teams (Project Managers, Pharmacovigilance, Regulatory Affairs, Clinical Operations) Model leadership for internal and external stakeholders in clinical trials and company strategy Interact with regulatory authorities to support development programs Responsabilità Degree in Medicine Excellent level of English (written and spoken) Good interpersonal skills Ability to build trust and confidence in teams/departments Ability to work independently Requisiti fondamentali Contract and salary proportional to experience #J-18808-Ljbffr

📌 Medical advisor (Italia)
🏢 Experteer Italy
📍 Italia