Teams at Alira Health

Conducts remote and onsite clinical trial monitoring visits, including qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, FDA, regulatory, and sponsor SOP compliance; reviews source documents, CRF data, regulatory binders, and trial documentation. Manages site issues, adverse event reporting, investigational product accountability, recruitment oversight, audit preparation, and monitoring reports. Collaborates with sponsors, sites, CRAs, project managers, data management, and cross-functional teams while mentoring CRAs and supporting CTMS activities.

Conducts remote and onsite clinical trial monitoring visits, including site qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, FDA, and SOP compliance; verifies source data, manages regulatory documentation, tracks investigational products, supports adverse-event reporting, and resolves site issues. The role also assists with monitoring plans, budgets, training, audits, sponsor communication, CTMS activities, CRA mentoring, and cross-functional coordination.

Conducts remote and onsite clinical trial monitoring visits, including site qualification, initiation, interim, and close-out activities. Ensures protocol, ICH GCP, regulatory, and SOP compliance; verifies source data, manages investigational product accountability, reviews regulatory documentation, and supports adverse event reconciliation. The role addresses site issues, recruitment, training, audits, budgets, CTMS activities, and sponsor communication while mentoring CRAs and coordinating with cross-functional clinical teams.