Jobs at Alira Health

Conducts and oversees clinical trial site monitoring across Belgium and the Netherlands. Responsibilities include investigator site visits, source data verification, regulatory documentation, protocol and ICH GCP compliance, adverse event reconciliation, audit preparation, monitoring plan support, and site issue resolution. The role also mentors CRAs, supports study training, coordinates cross-functional teams, manages monitoring budgets for standalone projects, and collaborates with sponsors, project managers, data management, and clinical trial technology teams.

Conducts independent clinical trial site monitoring across qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, regulatory, and documentation compliance; verifies source data, manages investigational product accountability, reviews regulatory files, and supports adverse-event reconciliation. Provides CRA mentoring and oversight, assists with monitoring plans and training, resolves site issues, supports recruitment, manages study budgets when applicable, and collaborates with sponsors, investigators, project teams, and data management. Freelancer must be based in Belgium or the Netherlands and travel between sites.

Executes global and local HEOR consulting projects, including cost-effectiveness models, budget impact models, local model adaptations, and early economic models. Manages project delivery, client and stakeholder engagements, analyses, reports, presentations, and team members. Supports business development, proposals, recruitment, coaching, and thought leadership through publications, abstracts, white papers, and conferences.

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.

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 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.