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Carle Health
Carle Health
Sponsor pentru viza H1BAsigurare de sănătateAsistență medicalăEducație
Carle Health este o organizație integrată de asistență medicală care răspunde nevoilor de sănătate ale comunității prin îngrijire medicală generală și servicii specializate, inclusiv oncologie, îngrijirea sistemului cardiovascular, pediatrie și sănătatea femeilor. Activitatea sa se extinde și în domeniile educației medicale și cercetării prin Carle Illinois College of Medicine, alături de inițiative de sănătate comunitară axate pe îmbunătățirea stării generale de bine. Operațiunile ample ale organizației din domeniul sănătății și educației susțin oportunități în echipe clinice, administrative, de cercetare și în alte echipe profesionale conexe.
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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.

USStatele Unite ale AmericiiILIllinois
23 $ – 39 $ / oră
La sediuNormă întreagăNivel mediuSeniorLimbă Obligatorie: englezăCercetare clinică

Descriere

  • 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.

Cerințe

  • 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.

Beneficii

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

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