Jobs at Alira Health

Supports clinical trial sites from approval through close-out without frequent travel. Responsibilities include preparing study and regulatory documents, supporting IRB submissions, ensuring site approvals, reviewing trial files and eCRF data, resolving queries, monitoring protocol and GCP compliance, training sites, assessing performance and accrual, and collaborating with field CRAs, data management, sponsors, and project managers.

Senior In-house Clinical Research Associates manage clinical sites from approval through close-out with limited travel. Responsibilities include preparing study and regulatory documents, supporting IRB submissions, ensuring site compliance with ICH GCP and FDA regulations, reviewing trial files and eCRF data, resolving data queries, training sites, monitoring performance and accrual, and collaborating with field CRAs, data management, sponsors, and project teams.

Manages clinical research studies from implementation through completion, ensuring compliance with approved budgets, timelines, ICH GCP guidelines, FDA regulations, and company SOPs. Serves as the primary sponsor contact, coordinates clinical functions and vendors, supervises clinical staff and Associate Project Managers, oversees study documentation and reporting, manages accrual and retention, supports audits and inspections, and communicates study status, risks, and milestones to stakeholders.

Supports clinical trial sites from approval through close-out without frequent travel. Responsibilities include preparing study and informed consent documents, supporting IRB submissions, maintaining regulatory files and the Trial Master File, reviewing remote eCRF data, monitoring protocol and GCP compliance, resolving data queries, training sites, assessing performance and enrollment, and collaborating with field CRAs, data management, sponsors, and project teams.

Supports consulting and research engagements for global healthcare clients through secondary research, quantitative and qualitative analysis, stakeholder interviews, evidence synthesis, and preparation of presentations, reports, models, proposals, and client communications. The Analyst collaborates with cross-functional teams on market access, pricing, patient engagement, real-world evidence, and health economics projects while developing knowledge of global healthcare systems.

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, 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.

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 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.