Carle Health je integrirana zdravstvena organizacija, ki skrbi za zdravstvene potrebe skupnosti s splošno zdravstveno oskrbo in specializiranimi storitvami, vključno z onkologijo, srčno-žilno oskrbo, pediatrijo in zdravstveno oskrbo žensk. Njeno delovanje vključuje tudi medicinsko izobraževanje in raziskave v okviru ustanove Carle Illinois College of Medicine ter pobude za zdravje skupnosti, osredotočene na izboljšanje splošnega dobrega počutja. Široko področje zdravstvenega in izobraževalnega delovanja organizacije podpira priložnosti v kliničnih, administrativnih, raziskovalnih in drugih strokovnih ekipah.
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.
Opis
- 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.
Zahteve
- 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.
Ugodnosti
- Comprehensive benefits package.
- Equal opportunity employer.
- Opportunities for professional growth and long-term careers.