Teams at Elite Clinical Network

Coordinates clinical research data and source documentation across clinical operations, contracts, study sites, and CTMS teams. Interprets clinical trial agreements, performs system data entry, reviews CTMS templates, develops standardized source documents, supports system integration, addresses audit findings, and provides site troubleshooting. Ensures documentation accuracy, regulatory compliance, data integrity, and alignment with protocol requirements across multiple studies.

Coordinate and support clinical trials by recruiting and consenting participants, collecting and processing specimens, performing basic clinical procedures, maintaining regulatory documentation and electronic case report forms, communicating with sponsors/IRBs, and ensuring protocol compliance and visit scheduling.

Coordinate and support clinical trials including recruitment, informed consent, specimen collection and handling, regulatory documentation, data entry in EDC/REDCap, scheduling visits, and communication with sponsors, monitors, and IRBs.