Teams at ObjectiveHealth

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.

Conduct clinical research protocols from patient identification, screening, randomization, and enrollment through clinic visits and study maintenance. Perform consenting, physical assessments, blood draws, medication administration, and ECGs. Maintain accurate data, eSource materials, regulatory documentation, adverse event tracking, and protocol compliance while coordinating with investigators, sponsors, monitors, and research teams.

Accurately enter, review, and maintain clinical trial data in EDC systems; verify and resolve data queries by comparing source documents; communicate with study staff; maintain documentation and audit trails; ensure compliance with study protocols, GCP, HIPAA, and regulatory requirements; support monitoring, audits, and database lock timelines.