Jobs at IQVIA

Lead planning and execution of independent GCP clinical audits across Europe, report findings, consult on regulations and corrective actions, maintain eQMS, review CAPAs/RCA, support QA initiatives, and train QA staff.

Assist the HR Business Partner team with talent development and training projects, support employee relations, system operations, and manage documentation.

The TMF Document Specialist ensures quality checks and compliance for trial master files, coordinates records retrieval, and trains staff in records management. Responsibilities include maintaining data integrity and managing documentation processes per regulatory standards.

The Snr Data Strategist oversees clinical systems documentation, implementation, and maintenance, providing technical support and data management, while ensuring compliance and continuous improvement within clinical research environments.

The Senior AI Engineer will design and develop advanced ML and NLP solutions for healthcare, collaborating across teams and mentoring juniors.

The Senior Site Activation Coordinator manages site activation activities for clinical trials, ensuring compliance with regulations and project requirements while coordinating with various teams and maintaining project documentation.

Serve as the primary client liaison, ensuring value from IQVIA products, managing interactions, and addressing complex inquiries in a fast-paced environment.

The Clinical Research Associate conducts site monitoring and management to ensure protocol adherence and quality data reporting while liaising with study teams and sites.

Assist in clinical research by supporting trial administration, maintaining documentation, aiding patient enrollment, and ensuring protocol adherence.

Lead Local Study Teams to deliver clinical studies, ensuring adherence to procedures, budgeting, timelines, and compliance with regulations. Oversee site selection, monitoring, and manage risks for successful study execution.

Perform routine in vitro ADME assays and sample analyses under supervision, follow SOPs and documentation standards, prepare reagents, operate and troubleshoot lab equipment, support basic data analysis and LIMS uploads, and assist process improvements to ensure high-quality, reproducible data.

Perform monitoring and site management to ensure compliance with study protocols, regulations, and sponsor requirements, including site visits and documentation.

The Key Account Manager will drive adoption of a new therapy by engaging with healthcare providers across Primary and Secondary Care, managing territory growth, and developing local treatment pathways.

The role involves leading Local Study Teams to deliver clinical studies, ensuring compliance, managing site activities, and coordinating with stakeholders.

The Clinical Research Associate will conduct monitoring visits, ensure compliance with study protocols, manage site communications, and support regulatory submissions and study management.

Support planning, coordination, and delivery of non-complex systems development projects. Maintain scope, schedules, and success metrics; monitor risks; execute communications; support cost tracking and change efforts; evaluate outcomes and recommend process improvements; contribute to reporting and stakeholder management under supervision.

Support clinical trials by performing administrative and clinical tasks: verify source documents, enter and quality-check data in EDC, maintain study and regulatory files (including FDA 1572), schedule subject visits, track visits in CTMS, and compile/submit study documentation on time while working with investigators and site staff.

The Analyst will conduct research and analysis, develop solutions for clients in life sciences, and support project execution while collaborating with teams.

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

Lead and execute manual and automated testing for client implementation projects. Create test plans, author and run test cases, track defects, collaborate across SDLC, troubleshoot issues, and escalate risks. Contribute to automation strategy and ensure compliance product quality.