Sub-Investigators (Sub-I)
Clinicians who perform trial-related procedures under the direction of the Principal Investigator.
Clinicians who perform trial-related procedures under the direction of the Principal Investigator.
Conducts clinical procedures, safety assessments and timed early-phase workflows, including PK sampling support.
Oversees IRB submissions, essential documents and GCP-aligned compliance processes across all studies.
Supports protocol procedures, participant scheduling, documentation and investigational product workflows.