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Clinical Study Operations Manager

90 000 - 110 000$
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
Clinical Study Operations Manager (Clinical Trials): Delivering clinical studies from startup through close-out with an accent on site onboarding, operational oversight, GCP compliance, and stakeholder coordination. Focus on training research sites, managing study risks and timelines, maintaining documentation discipline, and improving device and data-collection workflows.

Location: Fully remote anywhere in the U.S. Up to 10% travel required. In-person office hubs are available in Boston, New York, and Paris.

Salary: $90,000–$110,000 per year, plus equity, PTO, and other benefits.

Company

hirify.global develops at-home EEG and cardiopulmonary signal platforms for neurological, psychiatric, sleep, and central nervous system clinical development and diagnostics.

What you will do

  • Lead clinical study operations from startup through maintenance and close-out.
  • Coordinate study startup planning, communications, logistics, documentation, and data configuration.
  • Serve as the primary operational contact for clinical research sites and sponsors.
  • Train research sites on Beacon devices and study protocols to support accurate data collection.
  • Monitor timelines, protocols, quality standards, and operational risks across studies.
  • Coach ClinOps and Scientific teams on GCP compliance, documentation discipline, version control, and complaint management.

Requirements

  • 5+ years of experience in clinical project management or clinical operations.
  • Strong organizational, project management, written communication, and verbal communication skills.
  • Excellent English communication skills required.
  • Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements.
  • Knowledge of decentralized data collection, compliance, and clinical study oversight.
  • Proactive, detail-oriented, and able to manage multiple priorities in a fast-paced environment.

Nice to have

  • Additional language skills.
  • Interest in analytics, statistics, machine learning, and clinical trials.

Culture & Benefits

  • Contract-to-hire individual contributor role with asynchronous remote work practices.
  • Equity, paid time off, and other benefits.
  • Work focused on quality, scientific rigor, simplicity, composability, and self-service.
  • Culture emphasizing empathy for colleagues, stakeholders, users, and patients.
  • Up to 10% travel and access to in-person office hubs.

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