Human Subject Research Coordinator II
Core
Coordinates human subject research activities for investigator-initiated and pharmaceutical-funded clinical studies in the Epilepsy Division, managing participant recruitment, study visits, data collection, and regulatory compliance.
Role type
Mid-level human subject research coordinator (clinical trials)
Builds
Clinical research studies for children and adults with epilepsy
Domain
Healthcare / Clinical Research / Neurology
Required skills
Participant recruitment, study visit coordination, data entry, regulatory documentation management, IRB submission support, protocol adherence, database management, clinical task execution
Preferred skills
Phlebotomy, Human Subject Research Coordinator I experience, eRecord, iMedidata Rave, Zelta, REDCap, SOCRA/ACRP certification
Technologies
OnCore, Advarra Payment systems, Electronic Data Capture (EDC), iMedidata Rave, Zelta, REDCap
Responsibilities
Recruit participants and conduct study visits including assessments and clinical tasks; manage study start-up activities and consent forms; develop and manage databases and case report forms; prepare regulatory documentation and submit amendments for IRB approval; serve as liaison between research team, sponsors, and IRB; ensure compliance with federal, state, and institutional policies.
Seniority
Mid-level, hands-on IC