Teams at ObjectiveHealth

Lead and operate a clinical research site: coordinate industry-sponsored trials, enroll and care for patients, perform consenting and clinical procedures, ensure data quality and regulatory compliance, track AEs/SAEs, manage study setup and maintenance, liaise with PIs, sponsors, and monitors, and mentor site staff to meet enrollment and protocol goals.

Coordinate and manage IRB-approved clinical trials: identify, screen, randomize, and enroll patients; conduct clinic visits; consent and perform assessments (blood draws, ECG, medication administration); ensure data quality, regulatory compliance, AE/SAE tracking, and clear communication with PIs, sponsors, and monitors.

Coordinate and conduct IRB‑approved clinical trial activities including patient identification, screening, consenting, enrollment, clinic visits, specimen collection (blood draws), ECGs, medication administration, data entry, regulatory compliance, and communication with PIs, sponsors, and monitors.