Teams at TFS HealthScience

Conducts independent on-site and remote monitoring of clinical trial sites, including initiation, monitoring, and closeout. Ensures participant safety, informed consent, protocol compliance, data integrity, investigational product accountability, and accurate clinical documentation. Maintains site files and tracking systems, reports findings, supports audits and inspections, and collaborates with sponsors, investigators, and study teams. The role may mentor CRAs, support project activities, and deliver therapeutic-area training for ophthalmology studies.