Clinical Study Site Lead

🕒 Agosto 11

🇺🇸 Estados Unidos – Remoto (EUA)

⏰ Tempo Integral

🟠 Sênior

👻 Score fantasma 35%

O que significa: quão provável esta vaga está aberta sem contratação ativa.Como ler: 60% ou mais significa que achamos que é uma vaga fantasma. Pontuações mais baixas preocupam menos.Como pontuamos: tempo em aberto, republicações, vagas abertas vs tamanho do time, rapidez para fechar vagas, e se o salário está divulgado.Observação: é uma estimativa de dados públicos, não um julgamento da empresa. Vagas reais podem ter pontuação alta, então use como uma dica, não como um fato.

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GT Medical Technologies, Inc.

SiteLinkedInTodas as Vagas

51 - 200 funcionários

Fundada em 2017

🏭 Manufatura

🏥 Saúde

🔬 Ciência

Manufacturing • Healthcare • Science

A GT Medical Technologies, Inc. é uma empresa de tecnologia médica que desenvolve e comercializa a GammaTile Therapy, uma terapia de radiação direcionada cirurgicamente (STaRT) para tumores cerebrais operáveis. Seu produto GammaTile é um dispositivo de radioterapia implantável indicado para neoplasias intracranianas recém-diagnosticadas e recorrentes, projetado para fornecer radiação localizada ao leito do tumor no momento da cirurgia. A empresa apoia prestadores de cuidados de saúde e pacientes com recursos clínicos, centros de tratamento, pedidos e materiais educativos para melhorar os resultados para pacientes com tumores cerebrais.

Descrição

• Drive clinical study execution and operational excellence across GT Medical Technologies • Identify and collaborate with existing and potential clinical study sites and physicians • Initiate new and expand existing GammaTile study programs within institutions • Support rapid, focused study program startup and successful enrollment in sponsor-supported clinical studies, especially the BRIDGES trial • Build external relationships and provide leadership, data-driven site analysis, and cross-functional execution • Maximize clinical adoption, study patient enrollment, and GammaTile utilization • Coordinate efforts across Clinical Operations, Medical Affairs, and Commercial/Marketing • Establish and maintain relationships with neurosurgeons, radiation oncologists, physicists, medical/neuro oncologists, and administrative staff • Optimize recruitment strategies, enrollment forecasting, and study placement decisions • Identify, evaluate, and prioritize high-performing clinical study sites • Develop study site profiles covering patient populations, competing studies, research infrastructure, clinical disciplines, and investigator interest • Maintain communication with principal investigators, research coordinators, and regulatory personnel • Lead site stakeholder training and retraining to ensure protocol adherence • Develop patient throughput models and identify utilization growth opportunities • Support clinical and commercial growth through new institution onboarding and expanded participation by active institutions • Provide clinical insights as a clinical study subject matter expert • Support sales meetings, including Quarterly Business Reviews, as needed • Serve as a strategic liaison across Clinical Operations, Medical Affairs, Marketing, and Commercial teams • Partner with Clinical Operations to streamline feasibility, prioritize site selection, and track projected activation timelines • Lead and support the entire study site activation process, including SIV preparation and execution • Apply clinical study execution best practices • Train facility staff on protocol requirements and technology • Comply with company policies and procedures and protect access to PHI/ePHI for job-related functions • Perform other duties as assigned

🎯 Requisitos

• Bachelor’s degree in Healthcare, Biologic or Chemical Sciences, Medical Business, or a related field • 5+ years of experience in the Life Sciences industry with specific knowledge of clinical study operations • Strong clinical knowledge foundation and ability to engage in meaningful clinical dialogue with clinical study site representatives and clinicians • Excellent oral and written communication skills and audience awareness • Strong and diverse stakeholder management skills • Ability to think strategically while executing operationally • Independent problem-solving skills and ability to make decisions • Proficiency with Microsoft Office programs, including Outlook, Word, Excel, and PowerPoint • Willingness to work a flexible schedule • Ability to travel regularly for work • Satisfactory completion of comprehensive background screening • Satisfactory completion of drug screening, if applicable • Ability to occasionally pick up, carry, and move items up to 50 lbs • Availability for some evening and weekend work depending on workload • Frequent overnight travel required for work, events, and trainings

🏖️ Benefícios

• Full-time employment • Remote work in the West Region and Central-Mid-West Region • Professional/home office work environment • Company-provided training and retraining opportunities • Frequent overnight travel for work, events, and trainings