Description
QPS is hiring a Principal Investigator to lead assigned clinical trials and provide senior clinical oversight, continuity, and mentorship for PRN and Contract PIs. The role covers study conduct, regulatory compliance, subject safety, informed consent, eligibility verification, documentation, sponsor and IRB communication, and participation in monitoring visits, audits, and inspections. It is 100% office/lab based in Springfield, Missouri and requires an MD or DO, board certification, ICH-GCP knowledge, and experience leading clinical studies as a PI or Sub-Investigator; endocrinology expertise is helpful.
