
1001 - 5000 funcionários
Fundada em 1996
🏥 Saúde
💼 Consultoria
📦 Logística
Healthcare • Consulting • Logistics
PSI CRO AG é uma organização global de pesquisa por contrato (CRO) especializada na condução de ensaios clínicos. A empresa foca na entrega de ensaios clínicos pivotais de Fase 2 e Fase 3 em diversas áreas terapêuticas, incluindo Doenças Inflamatórias Intestinais, Oncologia, Hematologia, Doenças Infecciosas, Esclerose Múltipla e Doenças Raras. A PSI utiliza uma plataforma tecnológica proprietária para planejamento de ensaios clínicos e controle financeiro, garantindo que os estudos sejam conduzidos no prazo e dentro do orçamento. A empresa é reconhecida por sua expertise, qualidade, compatibilidade e confiabilidade, tendo sido premiada no CRO Leadership Awards por vários anos consecutivos.
🕒 5 dias atrás
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

1001 - 5000 funcionários
Fundada em 1996
🏥 Saúde
💼 Consultoria
📦 Logística
Healthcare • Consulting • Logistics
PSI CRO AG é uma organização global de pesquisa por contrato (CRO) especializada na condução de ensaios clínicos. A empresa foca na entrega de ensaios clínicos pivotais de Fase 2 e Fase 3 em diversas áreas terapêuticas, incluindo Doenças Inflamatórias Intestinais, Oncologia, Hematologia, Doenças Infecciosas, Esclerose Múltipla e Doenças Raras. A PSI utiliza uma plataforma tecnológica proprietária para planejamento de ensaios clínicos e controle financeiro, garantindo que os estudos sejam conduzidos no prazo e dentro do orçamento. A empresa é reconhecida por sua expertise, qualidade, compatibilidade e confiabilidade, tendo sido premiada no CRO Leadership Awards por vários anos consecutivos.
• Oversee, manage, and coordinate activities of project teams in designated countries • Ensure consistency of Clinical Operations processes across regions • Ensure study milestones are met by project teams at country and regional levels • Plan, implement, and manage projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents • Act as primary or secondary project management contact for project teams and PSI support services in designated countries • Review study status and provide progress reporting when delegated by the Project Manager • Collect and report project status updates for designated regions internally and externally • Develop and update project planning documents, essential study documents, and project manuals/instructions • Manage and report Key Performance Indicators for designated countries and clinical project team members • Ensure project timelines and subject enrollment targets are met • Coordinate study-specific and corporate tracking systems • Coordinate site contractual startup and budget negotiations • Establish communication lines within project teams and supervise clinical project team members' performance • Identify, escalate, and resolve resourcing and performance issues • Conduct and supervise therapeutic area training of project teams when delegated • Prepare presentations and conduct Investigator training • Ensure compliance with project-specific training matrices • Provide field training to Monitors tailored to project needs • Supervise site selection, site initiation, routine monitoring, and closeout visits • Oversee investigator and site payments, CRF data retrieval/upload, monitoring, and query resolution • Supervise project team preparation for study audits/inspections and resolution of findings • Coordinate supervised monitoring visits • Review site visit reports and ensure monitoring and reporting standards are met • Coordinate initial and follow-up Regulatory and Ethics Committee submissions and notifications • Oversee safety information flow and participate in feasibility research • Review and approve project-related expenses and timesheets when delegated by the Project Manager
• College/University degree in Life Sciences or an equivalent combination of education, training & experience is required • Prior experience in Clinical Research and on-site monitoring is required • Prior experience monitoring within the US • Experience as a Study Manager/Clinical Trial Manager with the ability to supervise project activities as a Regional Lead or equivalent is required • Experience in Oncology is required • Experience in GI is preferred • Full working proficiency in English • Proficiency in MS Office applications, including MS Project • Communication, presentation and customer-service skills • Ability to negotiate and build relationships at all levels • Team building, leadership and organizational skills
• Remote work option • Career growth opportunities • Opportunities to coordinate a variety of tasks and learn new things • Opportunity to grow with a rapidly growing company that puts its people first
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