Teams at CoMind

Owns clinical site monitoring across CoMind’s clinical program, conducting qualification, initiation, interim, and close-out visits. Responsibilities include source data review, query resolution, site performance oversight, issue escalation, CAPA support, investigator relationship management, IRB submissions, Trial Master File maintenance, regulatory support, site activation, and investigational product accountability. The role requires approximately 50% travel and collaboration with hospital clinicians and study teams.