Teams at Elite Clinical Network

Coordinates clinical trials and research studies by recruiting and enrolling participants, obtaining informed consent, collecting specimens, performing permitted basic clinical procedures, maintaining study data and regulatory documents, scheduling visits, and communicating with sponsors, monitors, and IRBs. Ensures protocol adherence, GCP compliance, investigational product accountability, and accurate documentation in case report forms and electronic databases.

Coordinates clinical trials and research studies, including participant recruitment, informed consent, visit scheduling, specimen collection and processing, clinical procedures, data entry, regulatory documentation, investigational product accountability, and communication with sponsors, monitors, and IRBs. Ensures protocols, ethical standards, GCP requirements, and visit windows are followed while maintaining accurate study records.

Leads end-to-end clinical study start-up activities from pre-award through Greenlight activation. Coordinates regulatory approvals, essential documents, contracts, budgets, vendors, recruitment readiness, and cross-functional handoffs. Tracks milestones, manages workflow systems, escalates delays, supports performance reporting, and drives process improvements. Serves as a subject-matter expert and mentor while partnering with leadership to improve study activation timelines and recruitment performance.