Clinical Research Coordinator — GI, Hepatology & Nutrition

Ohio State University; Columbus (OH); Presencial; USD 42 000 - 60 000; Tempo integral

Resumo da oferta

Ohio State University seeks a Clinical Research Coordinator for the Gastroenterology, Hepatology and Nutrition division. You will coordinate daily clinical studies, recruit and consent participants, and manage data collection in accordance with approved protocols.

This patient-facing, on-site role is based at University Hospital. Responsibilities include scheduling visits, monitoring safety, and ensuring regulatory compliance with IRB and sponsor requirements.

Qualificações

• Bachelor’s degree required in Biological Sciences, Health Sciences, Social Sciences or related field.
• 1 year of relevant clinical research experience required.
• Preferred: 2–4 years of experience; knowledge of medical terminology; certification in clinical research.

Responsabilidades

• Coordinate daily clinical research activities for Gastroenterology/Hepatology/Nutrition studies.
• Identify eligible patients by reviewing records, recruit, interview and enroll participants.
• Obtain informed consent and ensure consent process complies with regulatory and sponsor requirements.
• Schedule and coordinate patient visits, procedures and diagnostic testing per protocol.
• Monitor patients for adverse events and report to appropriate clinical personnel and sponsors.
• Assist with data collection, extraction, coding and analysis; generate reports and ensure data validity.
• Maintain compliance with IRB, FDA regulations and sponsor requirements.

Conhecimentos

Clinical Research

IRB Compliance

Data Collection

Regulatory Knowledge

Formação académica

Bachelor's Degree in Biological/Health/Social Sciences or related field

Ferramentas

Microsoft Office

EDC Systems

Descrição da oferta de emprego

Ohio State University seeks a Clinical Research Coordinator for the Gastroenterology, Hepatology and Nutrition division. You will coordinate daily clinical studies, recruit and consent participants, and manage data collection in accordance with approved protocols.

This patient-facing, on-site role is based at University Hospital. Responsibilities include scheduling visits, monitoring safety, and ensuring regulatory compliance with IRB and sponsor requirements.