Jobs at Alira Health

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.

Lead and perform site monitoring for clinical trials, ensuring GCP and protocol compliance. Oversee and mentor CRA team, manage monitoring visits (remote and onsite), prepare monitoring reports, verify source data and eTMF/TMF, handle SAE reconciliation and IP accountability, support site training and regulatory document collection, and coordinate with cross-functional teams to resolve site issues and meet study timelines and budgets.

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.

Responsible for independent site monitoring (initiation, monitoring, close-out), ensuring GCP/ICH compliance, managing ISF/TMF filing, IP accountability, safety event verification, site training, recruitment support, CRF/query resolution, and audit readiness. Collaborates with cross-functional teams and sponsors, prepares monitoring reports, and may manage study budgets for stand-alone projects. Frequent travel required to support on-site activities.

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.

Conduct secondary and primary research on pharmaceutical and biotech markets, support data analysis and financial modeling, prepare deliverable sections, coordinate interviews, and contribute to proposals, recruiting, and knowledge management while building therapeutic and industry expertise.

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.

Lead and manage complex life sciences consulting engagements: own project delivery, coordinate client and stakeholder interactions, guide analyses, produce reports and presentations, coach junior staff, support business development and thought leadership initiatives.

Lead and perform clinical site monitoring activities (qualification, initiation, interim, close-out) while mentoring CRAs, ensuring GCP/regulatory compliance, accurate CRF/eTMF documentation, SAE reconciliation, investigational product accountability, and resolving data queries. Support monitoring plans, site training, budgeting/billing, audit preparation, and CTMS collaboration across US and EU teams.

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.

Embedded in a consulting team, design and implement Python-based AI data pipelines, integrate LLM APIs, build and deploy LLM-powered agents and MCP servers, create reusable automation and multi-agent systems, translate business problems into AI solutions, support project scoping, and communicate technical work to non-technical stakeholders across healthcare and life sciences projects.

Support SSU Manager with clinical trial start-up activities: prepare and submit regulatory/ethics documents, localize ICFs, track timelines and metrics, maintain central study repositories, coordinate with sites, ECs and sponsors, and assist site identification and contract/indemnity processes.

Lead clinical study implementation and act as primary sponsor contact. Manage study functions (supply, IWRS/IXRS, data management, biostatistics, PV, central lab), supervise and train clinical staff, create and review study documents, ensure ICH GCP/FDA compliance, support TMF, prepare for audits/inspections, report study status and billing, and drive timely attainment of trial milestones.

Lead CRA provides oversight and mentorship to CRA teams, ensures GCP and protocol compliance, conducts onsite/remote monitoring visits, reviews CRF/source data and regulatory binders, supports hiring/onboarding and billing, assists with CTMS and quality processes, and liaises with cross-functional teams to resolve site issues and support study conduct.

Support cross-functional consulting teams by conducting secondary research, quantitative and qualitative analyses, preparing slide decks and reports, organizing stakeholder interviews, and contributing to proposals. Ensure analytical rigor, synthesize insights for pricing, market access, and real-world evidence projects, and collaborate with global teams while developing domain knowledge across healthcare systems.