Назад
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6 часов назад

Clinical Research Coordinator

37 800 - 94 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
junior/middle
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 Research Coordinator (Clinical Research): Managing clinical trials at an investigative site, from patient recruitment and informed consent to regulatory documentation, clinical procedures, and site audits with an accent on multi-therapeutic trial coordination and participant-facing research operations. Focus on performing phlebotomy and ECGs, processing lab specimens, maintaining eCRFs and CTMS records, and coordinating complex protocols.

Location: Fully on-site in Scottsdale, Arizona, United States

Salary: $37,800–$94,500 annualized base pay; actual compensation depends on qualifications, location, and schedule.

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries, with Avacare operating as a site management organization backed by hirify.global's global CRO resources.

What you will do

  • Coordinate 2–6 clinical trials across different therapeutic areas and complexity levels.
  • Support patient recruitment, informed consent, participant visits, and study activities from start to finish.
  • Perform vital signs, phlebotomy, ECGs, and laboratory specimen processing.
  • Maintain regulatory documentation and support site audits.
  • Work with investigators, sponsors, and monitors on trial execution.
  • Mentor junior staff and contribute to internal training.

Requirements

  • Hands-on clinical research experience at a clinical investigative site working with participants.
  • CRC I: 1–3 years of relevant experience; CRC II: at least 3 years as a Clinical Research Coordinator.
  • Knowledge of site operations and the drug development process.
  • Experience obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
  • Strong written and verbal communication, attention to detail, and time management.
  • Comfort using CTMS, eCRFs, and Microsoft Office tools.

Culture & Benefits

  • Collaborative environment focused on initiative, adaptability, and continuous learning.
  • Exposure to diverse clinical trials and multiple therapeutic areas.
  • Opportunities to work with investigators, sponsors, monitors, and junior staff.
  • Potential incentive plans, bonuses, and health and welfare benefits may be offered depending on the position.

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