Jobs 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.

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

Serve as physician of record and lead clinical oversight for Phase 2-4 trials, ensure participant safety and regulatory compliance, review and approve protocols and consent, conduct exams and safety assessments, mentor clinical research staff, and liaise with sponsors, monitors, and regulators.

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

Lead business development to drive revenue growth by identifying, qualifying, and closing complex deals with pharma, biotech, and CROs. Build senior client relationships, manage pipeline, negotiate contracts and pricing, collaborate cross-functionally for client onboarding, and mentor junior BD staff while informing product and go-to-market strategy.

Serve as physician of record and clinical lead for Phase 2-4 trials, ensuring patient safety, regulatory compliance (ICH-GCP, FDA, IRB), reviewing protocols and consent, conducting exams and safety assessments, mentoring the research team, and liaising with sponsors and regulators. Occasional travel for audits or site visits.