Назад
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5 дней назад

Clinical Research Coordinator

28 - 41$
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 (Clinical Trials): Coordinating clinical trial protocols, patient care, study visits, regulatory documentation, and clinical research data with an accent on Good Clinical Practice, protocol compliance, and source documentation. Focus on managing adverse event reporting, maintaining accurate CRF data, coordinating investigators and sponsors, and supporting IRB submissions.

Location: 600 N. Westmoreland, Lake Forest, Illinois, United States; ability to travel between hospital locations where research is conducted

Salary: USD 28.85–41.83 per hour

Company

hirify.global is a healthcare organization focused on patient-first care, clinical research, and improved health outcomes.

What you will do

  • Coordinate the logistical and operational aspects of assigned clinical trial protocols in accordance with Good Clinical Practice, standard operating procedures, and sponsor requirements.
  • Provide protocol-directed patient care, including investigational medication dispensing and study-related testing under physician supervision.
  • Schedule and coordinate study visits, procedures, medical coverage, vendor services, investigator meetings, and sponsor or monitor visits.
  • Serve as the primary contact for study participants and maintain communication with investigators, sponsors, research staff, and the IRB.
  • Collect and report adverse events, maintain source documentation and research files, and ensure protocol procedures are completed accurately.
  • Enter clinical data into case report forms, support IRB submissions, train research staff, and supervise document retention.

Requirements

  • Bachelor’s degree in a related field or equivalent experience in lieu of a degree.
  • At least two years of experience managing clinical research trials, with in-depth knowledge of protocol requirements and Good Clinical Practice.
  • Intermediate computer and internet skills.
  • Excellent patient care, customer service, written communication, and verbal communication skills.
  • Meticulous organizational skills and availability to travel between research hospital locations.

Nice to have

  • Three to five years of experience in clinical research trials.
  • ACRP or SOCRA certification.

Culture & Benefits

  • Patient-first workplace focused on better healthcare.
  • Full-time day-shift position.
  • Tuition reimbursement and loan forgiveness programs.
  • 401(k) matching and lifecycle benefits.
  • Background check required for newly hired team members.
  • Artificial intelligence tools may be used in parts of the candidate review process, while employment decisions are made by a person.

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