Research Coordinator - Clinical Research Institute - Per Diem 8 Hours Day (Non-Union, Non-Exempt)
Core
Assists investigators with clinical research studies, focusing on subject recruitment, data collection, scheduling, and regulatory compliance.
Role type
Clinical Research Coordinator
Builds
Clinical research studies and data sets
Domain
Healthcare / Clinical Research
Required skills
Regulatory compliance, data collection, subject recruitment, scheduling, documentation management, grant proposal support, sample processing, equipment ordering
Preferred skills
Medical terminology knowledge, CCRC certification
Technologies
MS Office, automated databases, CITI Program platforms
Responsibilities
Coordinate study participant activities including recruitment, screening, and appointments; collect and enter data from participants and medical records; maintain regulatory documents and consent forms; assist in grant proposal preparation and submission; ensure compliance with FDA, GCP, IRB, and HIPAA regulations; manage investigational product accountability; prepare for monitor visits and audits.
Seniority
Mid-level, hands-on IC