Teams 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.