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15 часов назад

18986-Sr Clin Research Coord

44 300 - 110 500$
Формат работы
onsite
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
18986-Sr Clin Research Coord (Clinical Research): Managing multiple clinical trials and coordinating participant-facing study activities from recruitment and informed consent through regulatory documentation and site audits with an accent on clinical procedures, protocol execution, and site operations. Focus on performing phlebotomy and ECGs, processing laboratory specimens, maintaining CTMS and eCRF records, and mentoring junior staff.

Location: Jefferson City, Missouri, United States; fully on-site

Salary: $44,300–$110,500 annualized base pay, depending on qualifications, location, and schedule.

Company

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

What you will do

  • Coordinate 2–6 clinical trials of varying complexity from study start through completion.
  • Recruit participants, obtain informed consent, and manage participant-facing trial activities.
  • Perform vital signs, phlebotomy, ECGs, and laboratory specimen processing.
  • Maintain regulatory documentation and support site audits.
  • Work with investigators, sponsors, and monitors on study 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.
  • Solid understanding of site operations and the drug development process.
  • Strong written and verbal communication, attention to detail, and time-management skills.
  • Experience with CTMS, eCRFs, and Microsoft Office tools.

Culture & Benefits

  • Exposure to multiple therapeutic areas and complex clinical protocols.
  • Collaborative environment focused on initiative, adaptability, and continuous learning.
  • Opportunity to work within a local Site Management Organization backed by a global CRO.
  • Health, welfare, and other benefits may be available depending on the position.

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