Jobs at IQVIA

Lead biostatistical activities for clinical studies: develop statistical sections of protocols, author SAPs, program datasets and TLFs, perform QC, manage lock/unblinding, mentor junior staff, liaise with clients and project teams, and help control study budgets and timelines.

Lead Data QA activities to test, validate, and ensure accuracy and integrity of data pipelines, warehouses, reports, dashboards, and analytics. Create test plans and cases, manage defects, coordinate cross-functional testing, present quality metrics, mentor junior staff, and drive continuous improvement and compliance support.

Support project planning, tracking, reporting, and governance for regulatory projects. Maintain plans, dashboards, risks, and documentation; coordinate finance activities, onboarding/offboarding, and stakeholder communications. Identify data issues and improve PMO tools and processes to ensure accurate, audit-ready delivery.

Support regulatory project delivery by maintaining plans, trackers, dashboards; monitor milestones, risks, and dependencies; prepare status reports and financial tracking inputs; ensure audit-ready documentation; coordinate onboarding/offboarding; escalate issues and drive standardization of PMO tools and reporting.

Contractor supports IVDR transition and regulatory compliance for IVD products across EMEA. Responsibilities include submission planning, product registrations, import notifications, change control coordination, regulatory database maintenance, milestone tracking, impact assessments, and stakeholder collaboration across cross-functional teams.

Support regulatory project delivery by maintaining plans, trackers, dashboards, and documentation; monitor milestones, risks, and issues; prepare status reports and metrics; coordinate onboarding/offboarding; partner with finance for effort tracking and forecasting; and improve PMO tools, governance, and reporting.

Design, build, and maintain Python automation for data validation and ETL checks. Perform data exploration, profiling, cleaning, and standardization. Write and optimize SQL queries, document validation logic, and collaborate with data engineers and QA teams to ensure data integrity across sources.

Lead and coach Agile teams by facilitating Scrum ceremonies, supporting Product Owners, managing scope, risks, stakeholders and delivery for moderately complex projects, enforcing Definition of Done, removing impediments, and reporting on metrics.

Designs and builds clinical study databases and eCRFs, creates edit specifications and EDC build components, manages study configuration in InForm, leads review meetings, communicates project risks, supports multiple concurrent studies and platforms, and contributes to process improvements and project financials for programming shared services.

Conduct on-site and remote monitoring for Phase I-IV clinical trials: site selection, initiation, monitoring, close-out visits, source data verification, investigational product accountability, data query resolution, report preparation, and liaison between IQVIA and investigators. Provide training, mentor junior CRAs, and ensure compliance with GCP/ICH and sponsor requirements.

Design and configure clinical study databases in InForm, interpret protocols, build and update eCRFs, create edit specification documents, define EDC components and rights/roles, attend design/review meetings, manage risks and training, and ensure timely, quality delivery of study design components.

Develop and implement Medidata Rave edit checks and custom C# functions from data validation specifications, perform post-production changes, build internal quality tools (Excel/Visual Studio), troubleshoot operational issues, and collaborate with CDM and corporate teams to meet timelines and deliverables.

The intern will assist in writing consulting project documentation, recording meeting minutes, organizing data, and supporting team members in report writing and other tasks.

Manage a team responsible for US GAAP accounting and statutory reporting, ensuring compliance, conducting audits, and supporting tax provisions.

The Senior Clinical Research Associate is responsible for site management and monitoring, protocol training, and maintaining recruitment and monitoring visit reports, working closely with a single sponsor.

As a Clinical Trials Assistant, you will support clinical teams by maintaining clinical documentation, assisting Clinical Research Associates, managing compliance, and handling administrative tasks related to clinical trials.

Drive volume and market-share growth for assigned pharmaceutical GI products within a territory by building relationships with healthcare providers, delivering sales presentations, managing samples and promotional materials per FDA/PDMA guidelines, documenting activity in the sales automation system, and completing required product training.

Lead a portfolio of patient support and hub service programs, oversee directors and managers supporting ~100–250 employees, maintain executive client relationships, drive strategic account planning and business development, monitor operational and financial performance, ensure contractual delivery, and collaborate cross-functionally to optimize service delivery and growth.

Provide executive leadership for large-scale nursing and patient support programs, ensuring client satisfaction, operational performance, and financial objectives. Build executive client relationships, mentor directors, support business development, and collaborate with cross-functional teams to drive innovation, quality, and growth across field-based and virtual nursing teams of ~100–250 employees.

Lead design and delivery of AI solutions for pharmaceutical R&D, leveraging foundation models, LLMs, RAG, agentic AI, knowledge graphs, and data architecture. Drive data integration, governance, model selection, evaluation, and production deployment while advising stakeholders, running workshops, and developing reusable methodologies to scale trustworthy, explainable AI in regulated life sciences environments.