Jobs at IQVIA

The Quality Manager implements the global Quality Plan, ensures compliance with standards, manages quality improvement initiatives, and supports stakeholders in adherence to clinical practices and regulations.

Responsible for developing and implementing learning and capability activities for TMF and CDGM services, ensuring alignment across organizational stakeholders and supporting document management practices.

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 TMF Specialist coordinates records management across projects, ensures compliance with SOPs, and manages project documentation while training team members.

The National Sales Manager will lead a sales team promoting an oral therapy for Multiple Sclerosis, develop sales strategies, oversee customer relationships, and collaborate with marketing and medical teams.

As an Associate Consultant, you will support project teams with market research, data analysis, and client project participation to develop healthcare solutions.

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

Lead the Centralized Monitoring team to oversee clinical deliverables, optimize project delivery, manage resources, and contribute to analytics strategies while ensuring compliance with SOPs and regulations.

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

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 role involves strategic leadership in expanding market share, managing teams, maintaining client relationships, and overseeing sales activities in the EMEA region for biopharma clients.

Lead the data onboarding function, translating complex healthcare data requirements into actionable plans, overseeing initiatives, and ensuring operational rigor, risk management, and continuous improvement.

The Revenue Coordinator ensures accurate posting and reconciliation of payments for transplant procedures, maintains records, resolves discrepancies, and supports revenue cycle operations.

The Staff Architect will lead technical vision and architectural strategy for MediaOS, ensuring scalable systems that align with business goals while mentoring teams and managing cross-product dependencies.

The Central Monitor performs centralized monitoring, evaluates clinical data quality, interacts with sites, and assists with data analytics. They ensure project compliance and escalate issues when necessary.

The Clinical Research Associate performs site selection, monitoring, and close-out visits, evaluates site practices, manages regulatory submissions and collaborates with study site experts.

The Data Analyst will perform strategic data analysis, evaluate secondary data, and create reports for pharmaceutical clients. Fluency in German and knowledge of SAS is required.

The Clinical Scientist will oversee and ensure data quality in clinical trials, conduct protocol reviews, develop training materials, and communicate with stakeholders.

The Principal Statistical Programmer provides statistical programming support across clinical development, ensuring compliance with CDISC standards and regulatory submissions, and leading high-quality programming efforts.