Carle Health
Carle Health
Carle Health ir integrēta veselības aprūpes organizācija, kas rūpējas par kopienu veselības vajadzībām, nodrošinot vispārējo medicīnisko aprūpi un specializētus pakalpojumus, tostarp onkoloģiju, sirds un asinsvadu aprūpi, pediatriju un sieviešu veselības aprūpi. Tās darbība ietver arī medicīnas izglītību un pētniecību, ko īsteno Carle Illinois College of Medicine, kā arī kopienas veselības iniciatīvas, kuru mērķis ir uzlabot vispārējo labklājību. Organizācijas plašā veselības aprūpes un izglītības darbība nodrošina iespējas klīniskajās, administratīvajās, pētniecības un citās saistītās profesionālajās komandās.

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.

Apraksts

  • 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.

Prasības

  • 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.

Priekšrocības

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

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