Teams at ObjectiveHealth

Coordinate and manage IRB‑approved clinical trial activities including patient identification, screening, enrollment, and clinic visits. Perform patient care tasks (consent, assessments, blood draws, med administration, ECG), ensure regulatory compliance, accurate data entry, AE/SAE tracking, maintain eSource and study documentation, and communicate with PIs, sponsors, and monitors.

Coordinate and execute IRB-approved clinical trial activities including patient identification, screening, consent, enrollment, clinic visits, specimen collection (phlebotomy), ECGs, medication administration, regulatory compliance, eSource/data entry, AE/SAE tracking, and communication with PIs, sponsors, and monitors to ensure protocol adherence and efficient study conduct.

Lead and operate clinical research sites: oversee study setup and maintenance, screen and enroll patients, conduct clinic visits and direct patient care (consent, assessments, blood draws, ECG, med administration), ensure regulatory compliance and clean data, manage AE/SAE reporting, coordinate with PIs, sponsors, monitors, and drive site performance.