Experteer OverviewIn 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 / BenefitsContribute to design,



execution and analysis of clinical trials in oncology and rheumatologyProvide expert guidance in designing and writing clinical trialsSupport monitoring of efficacy and safety by reviewing data and feeding analysis datasetsReview regulatory and pharmacovigilance documentationInteract with Principal Investigators and clinical site staff to advance trialsDisseminate scientific knowledge through publications and conferencesCollaborate with cross‐functional teams (Project Managers, Pharmacovigilance, Regulatory Affairs, Clinical Operations)Model leadership for internal and external stakeholders in clinical trials and company strategyInteract with regulatory authorities to support development programsResponsabilitàDegree in MedicineExcellent level of English (written and spoken)Good interpersonal skillsAbility to build trust and confidence in teams/departmentsAbility to work independentlyRequisiti fondamentaliContract and salary proportional to experience
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📌 Quality and Training Advisor (Italia)
🏢 Experteer Italy
📍 Italia