Teams at ObjectiveHealth

Enters, reviews, and maintains clinical trial data in EDC systems. Verifies source documents, resolves data queries, corrects discrepancies, maintains audit trails, and supports quality control, monitoring visits, audits, and regulatory compliance while protecting participant confidentiality.

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.