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2 дня назад

Clinical Research Coordinator (Oncology)

72 645 - 84 339$
Формат работы
onsite
Тип работы
fulltime
Грейд
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 (Oncology): Coordinating oncology clinical trials and supporting participants throughout screening, enrollment, treatment, and follow-up with an accent on informed consent, protocol compliance, regulatory documentation, and patient safety. Focus on reviewing adverse events, maintaining study records, preparing IRB materials, shipping specimens, and supporting monitoring and audit visits.

Location: Winchester, Virginia, United States; full-time onsite, Monday–Friday

Salary: $72,645–$84,339 per year

Company

hirify.global supports community-based oncology practices with resources for cancer care, clinical research, and professional development.

What you will do

  • Screen potential participants for protocol eligibility, present trial information, support informed consent, and enroll participants.
  • Coordinate participant visits and care in compliance with clinical trial protocols.
  • Review participant condition changes, adverse events, concomitant medications, treatment response, and protocol compliance with providers.
  • Maintain accurate clinical, regulatory, and study documentation, including adverse event reports, protocol worksheets, IRB documents, and continuing review reports.
  • Manage investigational product accountability, specimen packaging and shipment, provider orders, and protocol-specific billing information.
  • Support monitoring and auditing visits, staff education, quality improvement initiatives, study reporting, and research leadership activities.

Requirements

  • Associate degree in a clinical or scientific discipline, or an equivalent combination of education, clinical research experience, and applicable certification.
  • At least three years of experience as a Clinical Research Coordinator in a clinical research setting.
  • Experience with informed consent, participant visit coordination, regulatory documentation, adverse event reporting, and sponsor monitoring support.
  • Ability to work in a traditional office and clinical environment, including extended standing and walking and occasional lifting of up to 40 pounds.
  • Ability to work onsite in Winchester, Virginia, Monday through Friday.

Nice to have

  • Bachelor's degree in a clinical or scientific discipline.
  • Oncology clinical research experience.
  • SoCRA (CCRP) or ACRP certification.
  • Hazmat and/or IATA training.

Culture & Benefits

  • Mission-driven environment focused on patient care and scientific advancement.
  • Values centered on respect, excellence, teamwork, integrity, and compassion.
  • Community-based practice culture supported by the resources and stability of a larger oncology network.
  • Professional growth opportunities and required training and education programs.
  • Reasonable accommodations are available for qualified individuals with disabilities.

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