Jobs at Elligo Health Research, Inc.

Coordinates multiple clinical trials from study startup through closeout, including participant scheduling, informed consent, recruitment, study procedures, source documentation, data entry, query resolution, regulatory documentation, specimen handling, safety reporting, and monitoring visits. Ensures compliance with protocols, IRB requirements, GCP, ALCOA principles, SOPs, and participant safety standards while communicating with sponsors, clinics, vendors, and study teams.

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.