Clinical Research Coordinator- Clinical Research and Sponsored Programs
Core
Recruits and screens clinical research patients, obtains informed consent, collects and analyzes clinical data, and ensures regulatory compliance for clinical trials.
Role type
Clinical Research Coordinator
Builds
Clinical trial data and regulatory documentation
Domain
Healthcare / Clinical Research
Required skills
Medical terminology, Clinical research protocols, Data entry and documentation, Patient recruitment and screening, Informed consent processes, Regulatory compliance, Data analysis, Time management
Preferred skills
Certified Clinical Research Professional (CCRP), Epic Research Module
Technologies
Epic Research Module, Microsoft Word, Excel, Access
Responsibilities
Recruits and screens clinical research patients for protocol eligibility; Obtains informed consent through patient education; Performs data collection and analysis of test results; Serves as liaison for patients, physicians, and regulatory bodies; Prepares new study applications and informed consent documents; Coordinates with physician offices for billing compliance and drug accountability.
Seniority
Mid-level, hands-on IC