Teams at Civia Health

Lead daily operations of a clinical research site: manage coordinators and staff, oversee participant scheduling and visit flow, execute Phase II-IV studies, ensure protocol adherence, data integrity, regulatory compliance and audit readiness, train on clinical systems, liaise with IT and vendors, monitor performance, and drive process improvements.

Serve as physician of record and lead clinical oversight for Phase 2-4 trials: review/approve protocols and consent, perform exams and safety assessments, ensure ICH-GCP/FDA/IRB compliance, mentor clinical research staff, and engage sponsors/monitors. Occasional travel for audits or site visits.

Serve as physician of record and lead clinical oversight for Phase 2-4 trials: approve protocols and consent, perform exams and safety assessments, ensure ICH-GCP/FDA/IRB compliance, mentor research staff, and engage sponsors and regulators. Occasional travel for audits or site visits.