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9 дней назад

Imaging Manager, Clinical Operations (MedTech)

120 000 - 150 000$
Формат работы
remote (только USA)
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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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