Jobs at Alira Health

Conducts remote and onsite clinical trial monitoring visits, including site qualification, initiation, interim, and close-out activities. Ensures protocol, ICH GCP, regulatory, and SOP compliance; verifies source data, manages investigational product accountability, reviews regulatory documentation, and supports adverse event reconciliation. The role addresses site issues, recruitment, training, audits, budgets, CTMS activities, and sponsor communication while mentoring CRAs and coordinating with cross-functional clinical teams.

Conducts remote and onsite clinical trial monitoring visits, ensuring protocol, ICH GCP, FDA, regulatory, and sponsor SOP compliance. Reviews source documents, CRF data, regulatory binders, and trial files; manages investigational product accountability, adverse event reconciliation, site issues, recruitment, and audit preparation. Supports monitoring plans, budgets, training, CTMS activities, sponsor communication, and CRA mentoring while coordinating with cross-functional clinical teams.

Conducts remote and onsite clinical trial monitoring visits, including qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, FDA, regulatory, and SOP compliance; verifies source data and investigational product accountability; reviews regulatory documents; manages site issues, adverse event reconciliation, recruitment, and audit preparation. Supports monitoring plans, budgets, training, CTMS maintenance, CRA mentoring, sponsor communication, and cross-functional issue resolution.

Conducts remote and onsite clinical trial monitoring visits, including site qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, FDA, regulatory, ethical, and SOP compliance; verifies source data, manages investigational product accountability, reviews regulatory documents, supports recruitment, resolves site issues and data queries, and prepares monitoring reports. The role also supports monitoring plans, audits, budgets, CTMS activities, CRA training, mentoring, and sponsor-site communication.

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 across the Netherlands and Belgium, including qualification, initiation, interim, and close-out visits. Ensures protocol, ICH GCP, regulatory, documentation, data, and investigational product compliance. Reviews monitoring reports, supports recruitment and training, resolves site issues, manages study budgets, prepares audits, and coordinates with sponsors and cross-functional teams. Provides CRA oversight, mentoring, onboarding, and leadership while maintaining accurate trial records and data quality.

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.

Lead PMO initiatives and medium-to-large projects to improve processes, implement enterprise software, track KPIs, and ensure IT governance. Drive cross-functional stakeholder communication, mentor team members, and present performance updates to leadership while managing IT and business process integration.

Lead the PMO to translate strategic goals into operational plans, oversee project portfolio and M&A integrations, track financial and KPI performance, implement governance and process improvements, drive cross-functional alignment, mentor PMO staff, and deliver reports and dashboards to senior leadership to ensure successful execution of corporate initiatives.

Lead corporate clinical development operations and cross-functional teams to execute clinical trials and advance the development pipeline. Oversee clinical, nonclinical, regulatory, quality, CMC/manufacturing, and program management functions, ensure regulatory compliance (GCP/GLP/GMP/ICH/FDA), manage external CRO/CDMO partnerships, and drive operational strategy, budgeting, and risk mitigation. Serve on the Executive Leadership Team and support investor, board, and business development activities.

Support M&A and transaction advisory projects by conducting market and company research, preparing marketing materials (teasers, IMs, presentations), screening and shortlisting targets, assisting with financial valuations (multiples, DCF), preparing proposals and client reports, and monitoring industry and M&A developments.

Lead and support clinical trial start-up and coordination activities under PM oversight, including regulatory/ethics submissions, TMF/ISF management, vendor and site invoicing tracking, CTMS updates, mentoring junior coordinators, and participating in meetings and audits to ensure GCP-compliant study delivery on time and budget.

Lead and execute project workstreams for life sciences clients including market access, pricing, strategy, and commercial assignments. Perform primary/secondary research, quantitative modelling, report and presentation development, manage small teams (2-3), support business development, and ensure high-quality deliverables across global teams.

Lead and own project streams for market access, pricing, strategy, and commercial engagements in pharma/MedTech/DHS. Conduct primary and secondary research, quantitative modelling, produce client deliverables, present findings, manage small teams (2-3), and support business development and internal initiatives.

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 site monitoring for clinical trials including initiation, interim, and close-out visits (remote and onsite); review and document CRF/source data, manage regulatory binders, investigational product accountability, SAE reconciliation, QA/eTMF activities, mentor and train CRAs, support monitoring plans, budget/billing, and cross-functional issue resolution to ensure GCP and protocol compliance.

Conduct and oversee site monitoring for clinical trials including initiation, interim, and close-out visits (remote and onsite), source data verification, eTMF/CRF review, investigational product accountability, SAE reconciliation, site training and mentoring, regulatory compliance (ICH GCP/FDA/local), study documentation, and collaboration with sponsors and cross-functional teams to ensure protocol adherence and data quality.

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.

Support life-sciences strategy engagements by conducting market assessments, benchmarking, primary interviews, and data synthesis. Produce client deliverables including presentations and Excel models, translate analyses into strategic recommendations, and develop sector expertise across Biotech, Pharma, and MedTech.

Lead high-level life sciences client engagements, drive business development and corporate initiatives, generate and defend proposals, mentor teams, shape practice strategy and thought leadership, and contribute to M&A and cross-practice opportunities.