Teams at ObjectiveHealth

Serve as Sub-Investigator for assigned clinical trials, ensuring protocol compliance and subject safety. Perform and document physical exams and medical assessments, provide medical oversight throughout trial phases, collaborate with site staff and sponsors, participate in monitoring and audits, and maintain adherence to GCP, ICH, FDA regulations and internal SOPs.

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.

Coordinate IRB-approved clinical trial activities including patient identification, screening, consenting, enrollment, clinic visits, assessments, blood draws, ECG, medication administration, data entry, regulatory compliance, and communication with PIs, sponsors, and monitors.