Clinical/Translational Research Coordinator II
Core
Coordinates approval processes and conduct of clinical/translational research protocols to maintain integrity and quality in accordance with policies and regulations.
Role type
Clinical/Translational Research Coordinator
Builds
Clinical/translational trials
Domain
Healthcare / Clinical Research
Required skills
Regulatory compliance, IRB proposal preparation, Data entry on case report forms, Specimen shipping, Informed consent process, Study recruitment, Equipment procurement, Study invoicing management
Preferred skills
Qualitative and quantitative research methods, Protocol development, Project coordination
Technologies
Electronic case report forms, Shipping guidelines
Responsibilities
Prepare IRB research proposals, amendments, and adverse event reports; Maintain regulatory documentation for trials; Screen and recruit eligible study participants; Record data from source documentation to case report forms; Package and ship study specimens; Manage study invoicing and billing compliance; Facilitate informed consent processes; Participate in sponsor and regulatory site visits.