Emergency Medicine Clinical Research Coordinator

The Ohio State University Wexner Medical Center; Columbus (OH); On-site; USD 55,000 - 75,000; Full time

Job summary

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Department of Emergency Medicine.

This role involves identifying eligible patients, recruiting, enrolling, obtaining informed consent, and ensuring consent processes comply with regulatory and sponsor requirements.

Qualifications

• One year experience in a clinical research capacity.
• Knowledge of IRB, FDA, and sponsor regulations.
• Ability to collect and manage clinical data.

Responsibilities

• Coordinate and perform daily clinical research activities per protocol.
• Recruit, interview and enroll patients; obtain informed consent and ensure consent process compliance.
• Educate patients and families on purpose, goals and processes of the clinical study.
• Coordinate scheduling and follow-through of patient care appointments and tests.
• Assist in collection, processing and evaluation of biological samples.
• Administer questionnaires and monitor adverse reactions to study treatments.
• Notify appropriate clinical staff and sponsors about adverse events and regulatory statuses.
• Assist with data extraction, coding and reporting to verify data validity and protocol compliance.

Skills

Clinical research coordination

Regulatory compliance

Informed consent

Education

Bachelor's degree in biological/health/medical field

Job description

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Department of Emergency Medicine.

This role involves identifying eligible patients, recruiting, enrolling, obtaining informed consent, and ensuring consent processes comply with regulatory and sponsor requirements.