Clinical Study Site Lead

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GT Medical Technologies, Inc.

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 2017

🏭 Manufacturing

🏥 Healthcare

🔬 Science

Manufacturing • Healthcare • Science

GT Medical Technologies, Inc. is a medical technology company that develops and commercializes GammaTile Therapy, a surgically targeted radiation therapy (STaRT) for operable brain tumors. Its GammaTile product is an implantable radiotherapy device indicated for newly diagnosed and recurrent intracranial neoplasms, designed to deliver localized radiation to the tumor bed at the time of surgery. The company supports healthcare providers and patients with clinical resources, treatment centers, ordering, and educational materials to improve outcomes for patients with brain tumors.

📋 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

🎯 Requirements

• 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.

🏖️ Benefits

• 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