data integrityvendor managementmedical devicesclinical operationsmedical imagingmriultrasoundctsop authoring
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Мало
$120к-150к/год
$120к$160кмедиана$270к
По похожим ролям (35) ~ $160к/год
70
Хорошая вакансия
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Обязанности четко описаны, а работа связана с медицинскими технологиями, но зарплата ниже медианы для похожих ролей, что снижает привлекательность вакансии.
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Ниже рынкаПонятные задачиПрактическая медицина
Оценка от Hirify AI
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Imaging Manager, Clinical Operations (MedTech): Leading imaging operations for preclinical and clinical medical device research programs with an accent on multi-modality imaging, image quality, vendor governance, and regulatory data readiness. Focus on managing imaging data flows, monitoring core lab performance, maintaining data integrity, and resolving submission and turnaround-time risks across clinical studies.
Location: Remote - Contiguous United States; 10–20% travel
Salary: $120,000–$150,000 annually
Company
hirify.global is a commercial-stage medtech company developing the Edison® System, a non-invasive histotripsy-based sonic beam therapy platform for liver tumors and future applications across multiple disease areas.
What you will do
Lead imaging operations across preclinical studies and pre-market/postmarket clinical trials, serving as the technical resource for ultrasound, MR, CT, fluoroscopy, angiography, and other imaging modalities.
Oversee image acquisition, quality control, image reads, and consistency across readers and clinical sites.
Partner with study leads and R&D teams to design imaging components of study protocols and maintain imaging SOPs, procedures, and data-handling standards.
Govern imaging repositories, including user access, platform updates, migrations, vendor transitions, and read-delay or downtime risk.
Manage core labs and imaging vendors, including deliverables, documentation, statements of work, budgets, turnaround times, and corrective actions.
Coordinate the traceable flow of imaging data from sites to core labs and study databases, track submissions and missing data, escalate risks, and support internal, sponsor, and regulatory audits.
Requirements
Bachelor’s degree in life sciences, biomedical engineering, or a related field, or equivalent experience.
10+ years of hands-on experience in preclinical or clinical research, with substantial direct experience across multiple imaging modalities.
Experience in a regulated research environment, ideally in medical devices, biotech, or a CRO setting.
Experience authoring SOPs and protocols and training or mentoring technical staff.
Experience managing vendor core labs and/or sponsor relationships, including reviewing statements of work and budgets.
Strong data integrity practices and experience managing data flow and documentation across sites, core labs, internal databases, and other stakeholders.
Experience tracking timelines, escalating risks, and coordinating imaging submissions and data transfers.
Excellent written and verbal communication skills, with the ability to present technical findings to cross-functional and external audiences.
Proficiency with Microsoft Word, Excel, PowerPoint, Outlook, and Teams.
Culture & Benefits
Remote work within the contiguous United States with 10–20% travel.
Full-time employment with health, dental, and vision insurance.
Life insurance and short-term and long-term disability insurance.
401(k), paid time off, and additional benefits.
Work at the intersection of cutting-edge science and real-world medical application.
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