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.

Lead and perform clinical site monitoring activities (initiation, interim, close-out) ensuring protocol, ICH GCP, and sponsor compliance. Provide oversight, mentoring and guidance to CRA team, review monitoring reports, manage site documentation (eTMF/TMF), resolve data queries with data management, support SAE reconciliation, assist in training and monitoring plan development, and coordinate cross-functional issue resolution and budgeting for assigned studies.

Lead and oversee site monitoring activities for clinical trials, mentor CRAs, ensure protocol/GCP/FDA compliance, perform onsite and remote visits, prepare monitoring reports, manage eTMF/TMF and CRF data quality, support site training, budgeting and contract tasks, and coordinate cross-functional issue resolution.

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.

Senior CRA responsible for independent site monitoring and oversight of clinical trials in France. Duties include site initiation, interim and close-out visits (remote and onsite), report writing, source data verification, eTMF/TMF QC, IP accountability, regulatory binder review, mentoring CRAs, supporting monitoring plans/training, resolving queries with data management, and ensuring GCP/regulatory compliance throughout the study lifecycle.