Teams at Elite Clinical Network

The Clinical Research Assistant supports clinical research studies through administrative, technical, and participant-focused tasks, ensuring data integrity and compliance with regulations.

Coordinate and support clinical trials including participant recruitment, informed consent, specimen collection and processing, data entry in EDC, regulatory documentation, scheduling visits, and communication with sponsors, monitors, and IRBs. May perform basic clinical procedures and ensure protocol compliance and investigational product accountability.

Serve as Principal Investigator or Sub-Investigator on Phase I-IV trials, perform exams and eligibility assessments, provide medical oversight and safety monitoring, maintain ICH-GCP/FDA-compliant documentation, support recruitment and retention, and collaborate with coordinators, sponsors, and monitors.