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Clinical Operations Manager (Healthcare)

9 917 - 14 917$
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify RU Global, списка компаний с восточно-европейскими корнями
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Мэтч & Сопровод

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Описание вакансии

Текст:
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TL;DR

Clinical Operations Manager (Healthcare): Managing the operational execution of clinical studies with an accent on study documentation, compliance frameworks, and site management. Focus on driving core operational milestones, ensuring GCP compliance, and coordinating cross-functional team efforts from study design to closeout.

Location: Dallas, Texas (Must not require employer sponsored work authorization now or in the future for employment in the United States)

Salary: $119,000 - $179,000

Company

hirify.global Health is a data platform and technology company purpose-built to power AI-enabled precision health solutions that accelerate research and improve care.

What you will do

  • Author and establish critical study documentation, including Clinical Protocols, Informed Consent Forms (ICFs), and participant-facing materials.
  • Implement study operational plans, including the Integrated Quality Risk Management Plan (IQRMP) and Study Monitoring Plan.
  • Manage clinical site operations, protocol deviations, adverse event evaluations, and IRB reporting.
  • Oversee electronic Trial Master Files (eTMFs) to ensure full GCP compliance, regulatory adherence, and audit readiness.
  • Manage research timelines across the business from inception to publication.
  • Provide project management support for projects furthering business strategy for evidentiary claim development.

Requirements

  • Bachelor's degree in a life sciences, healthcare, or technical field, or equivalent practical experience.
  • 4+ years of direct experience in clinical operations, clinical trial management, or a related operational role within healthcare or biotechnology.
  • Direct experience drafting clinical study documentation (protocols, ICFs) and managing eTMF systems.
  • Strong subject matter expertise working inside cross-functional (XFN) project or product teams.
  • Must not require employer sponsored work authorization now or in the future for employment in the United States.

Nice to have

  • Deep familiarity with GCP compliance, regulatory submission considerations, and clinical SOP development.
  • Project management certification.
  • Experience with JIRA.

Culture & Benefits

  • Competitive base salary with bonus, equity, and comprehensive benefits.
  • Opportunity to work at the intersection of technology, data science, and healthcare.
  • Collaborative environment within cross-functional teams focusing on precision health.

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