Clinical Study Site Lead

🕒 August 11

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

👻 Ghost score 39%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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 • 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

🎯 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 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

🏖️ Benefits

• 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