IQVIA
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Recently posted jobs
Healthtech
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.
Healthtech
Responsible for developing and implementing learning and capability activities for TMF and CDGM services, ensuring alignment across organizational stakeholders and supporting document management practices.
Healthtech
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.
Healthtech
The TMF Specialist coordinates records management across projects, ensures compliance with SOPs, and manages project documentation while training team members.
Healthtech
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.
Healthtech
As an Associate Consultant, you will support project teams with market research, data analysis, and client project participation to develop healthcare solutions.
Healthtech
Serve as the primary client liaison, ensuring value from IQVIA products, managing interactions, and addressing complex inquiries in a fast-paced environment.
Healthtech
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.
Healthtech
The Clinical Research Associate conducts site monitoring and management to ensure protocol adherence and quality data reporting while liaising with study teams and sites.
Healthtech
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.
Healthtech
Perform monitoring and site management to ensure compliance with study protocols, regulations, and sponsor requirements, including site visits and documentation.
Healthtech
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.
Healthtech
Lead the data onboarding function, translating complex healthcare data requirements into actionable plans, overseeing initiatives, and ensuring operational rigor, risk management, and continuous improvement.
Healthtech
The Revenue Coordinator ensures accurate posting and reconciliation of payments for transplant procedures, maintains records, resolves discrepancies, and supports revenue cycle operations.
Healthtech
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.
Healthtech
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.
Healthtech
The Clinical Research Associate performs site selection, monitoring, and close-out visits, evaluates site practices, manages regulatory submissions and collaborates with study site experts.
Healthtech
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.
Healthtech
The Clinical Scientist will oversee and ensure data quality in clinical trials, conduct protocol reviews, develop training materials, and communicate with stakeholders.
Healthtech
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.



