Jobs 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.

Conducts remote and onsite clinical trial monitoring visits, ensuring protocol, ICH GCP, FDA, regulatory, and sponsor SOP compliance. Reviews source documents, CRF data, regulatory binders, and trial files; manages investigational product accountability, adverse event reconciliation, site issues, recruitment, and audit preparation. Supports monitoring plans, budgets, training, CTMS activities, sponsor communication, and CRA mentoring while coordinating with cross-functional clinical teams.

Conducts remote and onsite clinical trial monitoring visits, including qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, FDA, regulatory, and SOP compliance; verifies source data and investigational product accountability; reviews regulatory documents; manages site issues, adverse event reconciliation, recruitment, and audit preparation. Supports monitoring plans, budgets, training, CTMS maintenance, CRA mentoring, sponsor communication, and cross-functional issue resolution.

Conducts remote and onsite clinical trial monitoring visits, including site qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, FDA, regulatory, ethical, and SOP compliance; verifies source data, manages investigational product accountability, reviews regulatory documents, supports recruitment, resolves site issues and data queries, and prepares monitoring reports. The role also supports monitoring plans, audits, budgets, CTMS activities, CRA training, mentoring, and sponsor-site communication.