Teams at Adams Clinical

Provide foundational site-level support for clinical trials: assist study start-up, screen and schedule participants, perform vitals/ECGs/specimen collection as trained, complete ALCOA+-compliant source documentation, enter data into EDC, maintain study binders and logs, support monitoring visits, and assist with investigational product accountability under direct supervision while ensuring regulatory and GCP compliance.

Provide entry-level support for site-based clinical trials including study start-up, participant screening and scheduling, vitals/ECGs/specimen collection (as trained), data entry into EDC, source documentation, regulatory and audit support, investigational product accountability exposure, and general study coordination under direct supervision to ensure GCP-compliant study execution.

Own end-to-end payroll for a multi-site, multi-state clinical organization using Rippling. Process semi-monthly and off-cycle payroll, maintain records, reconcile reports in Excel, respond to employee inquiries, support benefits and year-end tax processes, and maintain audit-ready compliance documentation.