Clinical Research Coordinator

Responsibilities

• Screen potential patients for protocol eligibility and maintain monthly screening logs
• Present trial concepts and details to patients and facilitate the informed consent process
• Coordinate study patient scheduling for tests and treatments required by the protocol
• Document changes in patient condition, adverse events, concomitant medications, and protocol compliance
• Report serious adverse events and protocol deviations to the sponsor and/or IRB per regulatory guidelines
• Dispense oral or IV study drugs via sponsor-provided portals and maintain pharmacy accountability logs
• Ensure accurate data collection, entry, query resolution, and timely submission of research data
• Prepare for study visits by reviewing protocols, consent forms, patient charts, and study-specific checklists
• Support principal investigators with monitoring visits, study updates, and query resolution
• Maintain regulatory compliance, staff delegation documentation, and HIPAA standards

Requirements

• High school diploma or GED required; BS degree in science or healthcare preferred
• Valid driver’s license and must live in the State of Alabama
• Knowledge of medical terminology, anatomy, physiology, clinical medicine, surgery, and oncology
• Excellent computer, written, and oral communication skills
• Strong organizational skills and ability to multitask and work independently
• Exceptional attention to detail and reading comprehension for complex study protocols
• Understanding of HIPAA, GCP, OSHA, CDC, and applicable regulatory guidelines