Teams at Alira Health

Conducts independent clinical trial site monitoring, including qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, regulatory, and SOP compliance; verifies source data and trial documentation; manages site issues, safety reporting, recruitment, budgets, and sponsor communication. Provides CRA oversight, mentoring, training, and quality feedback while collaborating with project management, data management, and cross-functional teams. The role requires autonomous monitoring activity management and travel to sites.

Conducts independent clinical trial site monitoring, including qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, regulatory, and SOP compliance; verifies source data, manages investigational product accountability, reviews regulatory documentation, and resolves site issues. Supports monitoring plans, audits, recruitment, training, budgets, sponsor communications, and CTMS activities. Provides CRA oversight, mentoring, onboarding, and leadership while coordinating with project management, data management, finance, sponsors, and investigators.

Open application for a global talent pool for future internships, entry-level, and project roles across clinical trials, data, biostatistics/statistical programming, project coordination, and quality assurance. University students and recent graduates are encouraged to submit CVs for Talent Acquisition review and consideration for matching opportunities.