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9 дней назад

Remote Visit Coordinator, US Regional Specialist

51 000 - 127 400$
Формат работы
remote (только USA)
Тип работы
fulltime
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
Remote Visit Coordinator, US Regional Specialist (Clinical Research): Coordinating remote and decentralized clinical trial visits across investigator sites, research clinicians, and internal study teams with an accent on documentation, clinician onboarding, systems administration, and visit logistics. Focus on maintaining study trackers, verifying regulatory documents, resolving operational issues, and ensuring compliance with GCP, ICH, HIPAA, and IQVIA SOPs.

Location: Home-based in the United States

Salary: $51,000–$127,400 annual base pay

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Coordinate remote and decentralized trial visits between investigator sites, remote research clinicians, and internal study teams.
  • Conduct outreach, onboarding, and study-specific training for investigator sites and research clinicians.
  • Process Visit Request Forms, assign clinicians, and coordinate visit logistics, supplies, equipment, and courier services.
  • Manage access to Study Hub, Thinking Cap, and other clinical trial systems.
  • Maintain site, visit, and clinician trackers and perform quality checks on uploaded documentation.
  • Act as the primary liaison, escalate issues, and support timely resolution across assigned studies.

Requirements

  • Bachelor’s degree or an equivalent combination of education, training, and experience.
  • Two years of research experience strongly preferred.
  • Strong written and verbal communication, presentation, interpersonal, problem-solving, organizational, and analytical skills.
  • Proficiency in Microsoft Word, Excel, PowerPoint, and clinical trial database systems.
  • Ability to coordinate multiple studies while following regulatory and institutional guidelines.
  • Must be based in the United States and able to work from a home-based setup.

Culture & Benefits

  • Full-time employment with health and welfare benefits potentially available.
  • Work supporting clinical research and innovative medical treatments.
  • Responsibilities follow FDA Good Clinical Practices, FDA regulations, and hirify.global standard operating procedures.
  • Equal opportunity employment environment.

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