Jobs at IQVIA

Lead startup strategy and execution for Remote Research Clinician services across multiple clinical studies. Partner with sponsors and cross-functional teams to design hybrid/decentralized visit models, develop startup plans, oversee process implementation, drive operational readiness, monitor progress, mitigate risks, support proposals, and promote continuous improvement in decentralized clinical trial delivery.

Serve as single point of contact for feasibility, site activation and maintenance for assigned studies. Review and prepare regulatory/site documents, track approvals, distribute completed materials, and maintain databases, tracking tools and project plans. Coordinate with Site Activation Manager, project teams and sponsors to ensure compliance with local regulations, SOPs and ICH/GCP.

Support CRAs and RSU teams by maintaining Trial Master File and clinical documentation, tracking CRFs and supplies, assisting with filing, distribution, archiving, and periodic file reviews; act as central project contact and occasionally assist on site visits after training.

Support delivery of clinical and RWE studies within an FSP model: develop study management plans, manage assigned study portions or sub-teams, monitor milestones, identify and mitigate risks, ensure quality and compliance (ICH GCP), coordinate vendors, support finances and change control, and drive best-practice and knowledge transfer across clinical and RWE pipelines.

Develop, fine-tune, evaluate, and deploy LLMs and agentic AI solutions using large healthcare datasets. Build data pipelines, distributed training and inference infrastructure, integrate models into platforms and workflows, apply best practices for reproducibility, benchmarking, safety, and regulated environments while collaborating across AI, engineering, and domain teams.

Support project planning, tracking, reporting, and governance for regulatory projects. Maintain plans, dashboards, risks, and documentation; coordinate finance, onboarding/offboarding, and stakeholder reporting; identify issues and improve PM tools and standards.

Lead delivery of oncology clinical studies: develop study plans, manage cross-functional teams and vendors, monitor progress and finances, mitigate risk, ensure regulatory compliance (ICH GCP), and communicate with stakeholders to meet timelines, quality, and contractual objectives.

The Clinical Trial Assistant supports Clinical Research Associates and Regulatory teams by managing trial documentation, communication, and administrative tasks to ensure compliance and timely delivery of study materials.

Lead complex global, multi-regional clinical trials from start-up through close-out for renal, obesity and/or MASH. Provide strategic sponsor partnership, oversee timelines, budgets, quality, risks and regulatory compliance, direct cross-functional teams, and drive operational delivery to achieve study objectives.

Support clinical trial delivery by assisting Project Leaders with scheduling, risk and issue management, project finances (EAC, expenses, invoices), vendor/PO processes, baseline/change control, eTMF filing compliance, eTraining, resource allocation, status reporting, and meeting coordination. Maintain dashboards and IQVIA systems data to enable timely decision-making and support audits and onboarding of project team members.

Manage country-level site activation for assigned studies: act as SPOC, perform feasibility/site identification/start-up activities, prepare and quality-check site and regulatory documents, maintain tracking systems, support IRB/submissions and contract/budget processes, coordinate timelines and contingency plans, and provide local expertise to project teams and sponsors.

Lead and oversee operational delivery of CNS clinical studies and programs from pre-award to close-out. Drive project strategy, client relationships, financial performance, risk mitigation, team leadership and cross-functional collaboration. Prepare integrated management plans, defend bids, manage change control, ensure regulatory and quality compliance, mentor junior staff, and promote continuous improvement across global study teams.

Paid full-time Health Economics intern supporting client projects (~40%) and a dissertation (~60%). Tasks include literature reviews, economic modelling, HTA and evidence-generation materials, client communication, and contributing to methodological initiatives while working with cross-European teams and subject-matter experts.

Lead and deliver supply chain and operations transformation projects for life sciences clients, performing quantitative and qualitative analysis, designing process and digital solutions, coordinating junior team members, supporting proposals and client workshops, and engaging with senior client stakeholders. Travel to client sites in Italy required.

Senior AI/ML Engineer to design, build, and scale production-grade LLM-powered, Agentic AI and RAG systems for healthcare and life sciences. Hands-on Python backend development, RESTful APIs and microservices, integrating frameworks like LangChain, optimizing models and performance, and translating prototypes into scalable enterprise deployments while collaborating with product and data teams.

Lead and manage biostatistical work for clinical trial projects: design statistical methods, write SAPs and sample size reports, develop/review analysis programs and datasets, produce statistical analysis reports, review CRF/database design, support randomization, mentor junior staff, ensure SOP compliance, and communicate results with study teams and clients.

Manage monthly and quarterly corporate consolidation and reporting, prepare topside journal entries, support SOX/audit requests, analyze complex accounting issues, assist with M&A accounting, and drive reporting process improvements and automation while partnering with finance teams and senior leadership.

Lead delivery of clinical studies or study components, managing cross-functional teams to meet contract, quality, timeline and financial goals. Oversee planning, risk management, vendor relationships, change control, stakeholder communication, and staff development while ensuring compliance with ICH GCP and corporate processes.

Ensure data integrity and high-quality outputs across syndicated data sources. Perform data quality checks, statistical analysis, process improvement, documentation, KPI tracking, exception resolution, and client support while collaborating with internal teams.

Ensure quality and timeliness of HPA commercial and Hospital Analyzer data: validate and analyze data using CRM and specified tools, investigate ward/production queries, create report specifications, perform checks and audits to ensure accurate client reports, and liaise between suppliers, local office and Manila production.