Deputy QPPV

Há 17 horas
Porto, Portugal IQVIA Inc Tempo integral 150 000 € - 230 000 € Contrato
IQVIA seeks a Medical Strategy Lead in Oncology-Clinical Development to provide strategic medical input across proposals, RFP responses, and client discussions. You will lead protocol design discussions, translate scientific insight into development plans, and guide teams through the lifecycle of clinical trials, collaborating with BD, Operations, and other COE leads to drive impactful outcomes. The role requires an MD in Oncology with board certification, 5–7 years of relevant experience, and

  • Deputy Qppv: Pharmacovigilance Lead

    Há 17 horas

    Porto, Porto, Portugal IQVIA Inc Tempo integral 150 000 € - 230 000 € Contrato

    Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence) Reading, Berkshire, United Kingdom Belgrade, Serbia Vienna, Austria Budapest, Hungary Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria Bucuresti, Romania Madrid, Spain Porto Salvo, Portugal Brussels, Brussels-Capital Region, Belgium Prague, Czech Republic Copenhagen,...

  • Deputy Qppv: Pharmacovigilance Lead

    Há 4 dias

    Porto, Porto, Portugal Iqvia Tempo integral 150 000 € - 230 000 € Contrato

    Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence) Reading, Berkshire, United Kingdom Belgrade, Serbia Vienna, Austria Budapest, Hungary Amsterdam, Netherlands Barcelona, Spain Sofia, Bulgaria Bucuresti, Romania Madrid, Spain Porto Salvo, Portugal Brussels, Brussels-Capital Region, Belgium Prague, Czech Republic Copenhagen,...

  • Regulatory Affairs

    Há 2 semanas

    Porto, Porto, Portugal Astrum Tempo integral

    Regulatory Affairs & Pharmacovigilance ManagerRegulatory Affairs & Pharmacovigilance ManagerWe are seeking aRegulatory Affairs & Pharmacovigilance Managerto lead our RA/PV team and ensure regulatory compliance and robust patient-safety systems across our clinical trials and client projects.Key ResponsibilitiesLead, develop, and support the RA/PV team,...

  • Regulatory Affairs

    Há 2 semanas

    Porto, Porto, Portugal Astrum Cro Tempo integral

    Regulatory Affairs & Pharmacovigilance ManagerRegulatory Affairs & Pharmacovigilance ManagerWe are seeking aRegulatory Affairs & Pharmacovigilance Managerto lead our RA/PV team and ensure regulatory compliance and robust patient-safety systems across our clinical trials and client projects.Key ResponsibilitiesLead, develop, and support the RA/PV team,...

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