Teams at Care Access

Supports GxP quality assurance and compliance across clinical research sites and decentralized trials. Responsibilities include reviewing regulatory documents, executing and tracking audits, managing CAPA plans, supporting external inspections, maintaining quality systems and compliance trackers, developing SOPs, advising clinical teams, delivering quality training, and promoting inspection readiness. The role also supports RFPs, AI quality initiatives, data accuracy, and GxP/non-GxP quality projects.

Coordinate virtual participant education, consent, retention, and study pre-screening for the Future of Medicine program. Deliver lab result education, perform e-consent, match participants to studies, document interactions per GCP/ALCOA-C, manage participant communications, and support referral follow-through while meeting quality and volume targets.

Support day-to-day AP/AR, billing, cash application, reconciliations, and reporting. Prepare and review invoices and vendor bills, research variances, resolve routine discrepancies, assist month-end close, and collaborate with cross-functional teams to maintain accurate financial records and controls.