Jobs at Alira Health

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.

Conduct site monitoring activities for clinical trials including initiation, interim, and close-out visits; ensure protocol/GCP compliance, source/CRF verification, SAE reconciliation, regulatory binder review, investigational product accountability, query resolution, audit prep, and reporting. Collaborate with in-house CRAs, project managers, and sponsors to support site performance and enrollment.

Lead and mentor the database programming (DBP) team to design, build, validate and maintain clinical study databases and data checks (SAS and computerized) from study startup through delivery, ensuring compliance with ICH/GCP and company standards, supporting data imports, mid-study changes, reporting, and process improvements.