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Carle Health
Carle Health
H1B vizasi homiysiSog‘liqni saqlashTa’limTibbiy sug‘urta
Carle Health umumiy tibbiy yordam, shuningdek onkologiya, yurak-qon tomir kasalliklari bo‘yicha yordam, pediatriya va ayollar salomatligi kabi ixtisoslashtirilgan xizmatlar orqali jamiyatning sog‘liqni saqlash ehtiyojlariga xizmat ko‘rsatuvchi integratsiyalashgan tibbiyot tashkilotidir. Tashkilot faoliyati Carle Illinois College of Medicine orqali tibbiy ta’lim va tadqiqotlarni, shuningdek umumiy farovonlikni yaxshilashga qaratilgan jamoat salomatligi tashabbuslarini ham qamrab oladi. Uning keng ko‘lamli tibbiy xizmat va ta’lim faoliyati klinik, ma’muriy, tadqiqot hamda boshqa tegishli professional jamoalarda imkoniyatlarni qo‘llab-quvvatlaydi.
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Kompaniyadagi ish o‘rinlari

Clinical Research Coordinator

Coordinate clinical trials across Carle Health’s Illinois healthcare system, from recruitment and regulatory submissions through data collection and study close-out.

USAmerika Qo‘shma ShtatlariILIllinoys
23 $ – 39 $ / soat
OfisdaTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaKlinik tadqiqot

Tavsif

  • Coordinate daily clinical trial activities with the Principal Investigator.
  • Oversee trials from study start-up through completion.
  • Support study development, feasibility reviews, preparation, and IRB submissions.
  • Evaluate patient populations and plan recruitment and enrollment strategies.
  • Recruit, screen, and oversee trial participants.
  • Collect and report trial data while maintaining source records.
  • Arrange and take part in study monitoring and audits.
  • Help prepare staff training materials and tools, and maintain training records.
  • Communicate with sponsors, participants, and the Principal Investigator.
  • Escalate instances of noncompliance to the appropriate oversight body.
  • Protect patient confidentiality in accordance with HIPAA.
  • Assist with study close-out, research articles, audit preparation, final reports, financial obligations, and archiving.

Talablar

  • Bachelor’s degree in health science or a scientific field.
  • Conduct clinical trials in accordance with good clinical and scientific practices.
  • Understand protocol requirements, participant visit schedules, and research plan execution.
  • Screen patients for protocol eligibility and manage informed consent.
  • Collect source documents, enter data, and complete case report forms.
  • Maintain regulatory documents according to sponsor requirements.
  • Understand HIPAA regulations and applicable laws.
  • Follow federal, state, and professional regulatory standards.
  • Participate in required training and education programs.

Imtiyozlar

  • Comprehensive benefits package.
  • Equal opportunity employer.
  • Opportunities for professional growth and long-term careers.

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MasofaviyTo‘liq stavkaSeniorTalab Qilinadigan Til: inglizchaYechimlar muhandisi
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