Teams at ObjectiveHealth

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.

Coordinate and manage IRB-approved clinical trial activities including patient identification, screening, consenting, randomization, enrollment, clinic visits, specimen collection, medication administration, ECGs, regulatory compliance, clean data entry, adverse event tracking, and collaboration with PIs, sponsors, and monitors to ensure protocol adherence and quality patient care.