Teams at Elligo Health Research, Inc.

Supports clinical trial execution through participant screening, recruitment, consent, data entry, clinical assessments, specimen collection and processing, laboratory testing, ECGs, vital signs, spirometry, study documentation, supply management, and follow-up coordination. Ensures compliance with protocols, regulations, SOPs, infection-control requirements, and participant safety while collaborating with coordinators, investigators, sponsors, and clinical research staff.

Coordinates multiple clinical trials by scheduling participants, collecting histories and source documents, entering data, resolving queries, and supporting regulatory documentation. Assists with recruitment, informed consent, study visits, specimen processing, adverse-event reporting, monitoring visits, and study closeout. Ensures protocol, IRB, GCP, SOP, and ALCOA compliance while collaborating with sponsors, sites, vendors, and internal study teams.