Research Coordinator - Clinical Research Institute - Per Diem 8 Hours Day (Non-Union, Non-Exempt)
Core
Coordinates clinical research studies by managing subject recruitment, scheduling assessments, collecting data, and ensuring regulatory compliance.
Role type
Clinical Research Coordinator
Builds
Clinical research studies and data sets for investigators
Domain
Healthcare / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | client delivery | physical/clinical work
Required skills
Subject recruitment, data collection and entry, regulatory compliance (FDA/GCP/IRB), scheduling, report generation, grant proposal support, investigational product accountability
Preferred skills
Medical terminology knowledge, CCRC certification
Technologies
MS Office, automated databases, CITI Program platforms
Responsibilities
Assist with organizing and scheduling assessments/tests to meet study protocol compliance; Participate in assessing patient eligibility and coordinating participant activities; Assist with data collection, recording, and preliminary analysis; Maintain accurate records including source documents and consent forms; Assist in preparation of grant proposals and regulatory submissions; Ensure consent process compliance with regulations; Provide ongoing education to study subjects; Assist in preparation for monitor visits and audits; Collaborate on investigational product accountability and sample processing.
Seniority
Mid-level, hands-on IC