Clinical Study Site Lead

🕒 il y a 10 jours

🇺🇸 États-Unis – Télétravail

⏰ Temps Plein

🟠 Senior

👻 Score fantôme 12%

Ce que ça veut dire : la probabilité que cette offre reste ouverte sans recrutement actif.Comment le lire : 60 % ou plus, on pense que c'est une offre fantôme. Un score plus bas est moins inquiétant.Comment on la calcule : ancienneté, republications, postes ouverts vs taille de l'équipe, rapidité de clôture, et si le salaire est indiqué.À noter : une estimation à partir de données publiques, pas un jugement sur l'entreprise. De vraies offres peuvent avoir un score élevé, alors prenez-le comme un indice, pas comme un fait.

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GT Medical Technologies, Inc.

Site WebLinkedInTous les Emplois

51 - 200 employés

Fondée en 2017

🏭 Fabrication

🏥 Santé

🔬 Science

Manufacturing • Healthcare • Science

GT Medical Technologies, Inc. est une entreprise de technologie médicale qui développe et commercialise la GammaTile Therapy, une thérapie par radiation ciblée chirurgicalement (STaRT) pour les tumeurs cérébrales opérables. Son produit GammaTile est un dispositif de radiothérapie implantable indiqué pour les néoplasmes intracrâniens nouvellement diagnostiqués et récurrents, conçu pour délivrer une radiation localisée au lit tumoral au moment de la chirurgie. L'entreprise soutient les prestataires de soins de santé et les patients avec des ressources cliniques, des centres de traitement, des systèmes de commande et des matériels éducatifs pour améliorer les résultats pour les patients atteints de tumeurs cérébrales.

Description

• Drive clinical study execution and operational excellence across GT Medical Technologies • Identify and collaborate with existing and potential clinical study sites and physicians to initiate or expand GammaTile study programs • Support rapid study program startup and enrollment in sponsor-supported clinical studies, especially the BRIDGES trial • Build and maintain relationships with neurosurgeons, radiation oncologists, physicists, medical/neuro oncologists, and administrative staff • Coordinate efforts across Clinical Operations, Medical Affairs, Commercial, and Marketing teams • Identify, evaluate, prioritize, and profile high-performing clinical study sites • Develop recruitment strategies, enrollment forecasts, study placement decisions, and patient throughput models • Maintain communication with principal investigators, research coordinators, and regulatory personnel • Lead site stakeholder training and retraining to support protocol adherence • Develop and help execute clinical and commercial growth strategies through new institution onboarding and expanded use by active institutions • Provide clinical insights and subject matter expertise to account performance and sales meetings • Serve as a strategic liaison across internal teams and existing clinical study partners • Partner with Clinical Operations on feasibility, site selection, and activation timelines • Lead and support study site activation, including SIV preparation and execution • Train facility staff on protocol requirements and technology • Comply with company policies and procedures and protect PHI/ePHI access • Perform other duties as assigned

🎯 Exigences

• Bachelor’s degree in Healthcare, Biologic or Chemical Sciences, Medical Business, or a related field • 5+ years of experience in the Life Sciences industry • Specific knowledge of clinical study operations • Strong clinical knowledge and ability to engage in meaningful clinical dialogue with 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 and decision-making skills • Proficiency with Microsoft Office programs, including Outlook, Word, Excel, and PowerPoint • Willingness to work a flexible schedule • Ability to travel regularly for work • Ability to satisfactorily pass comprehensive background screening • Ability to satisfactorily pass drug screening, if applicable • Frequent overnight travel required • Ability to occasionally pick up, carry, and move items up to 50 lbs.

🏖️ Avantages

• Full-time employment • Remote work in the West Region and Central-Mid-West Region • Flexible schedule • Professional or home office work environment • Company-provided work, events, and training travel • Clinical and cross-functional professional development through training/retraining opportunities