Job Overview
Location
Vienna, Austria
Job Type
Full-time
Category
HR & Recruiting
Date Posted
July 1, 2026
Full Job Description
đź“‹ Description
- • As a Clinical Research Associate I (CRA I) in IQVIA’s Clinical Site Management department, you will play a vital role in advancing groundbreaking medical treatments by ensuring clinical trials are conducted ethically, safely, and in full compliance with global standards. Based in Austria and working remotely, you will contribute to the development of innovative therapies across multiple therapeutic areas, supporting sponsors in bringing new medicines to patients worldwide.
- • Your day-to-day responsibilities will include conducting site selection, initiation, monitoring, and close-out visits for complex clinical trials; supporting subject recruitment planning; evaluating site practices for compliance with GCP and ICH guidelines; tracking regulatory submissions, recruitment progress, CRF completion, and data query resolution; and collaborating closely with study site experts and client representatives to ensure trial integrity and timely execution.
- • You will join IQVIA, a global leader in clinical research services, healthcare intelligence, and commercial insights, where you’ll be part of a dedicated Clinical Site Management team supported by strategic site relationship managers. This role offers deep integration into a wider clinical operations network focused on accelerating the development of life-changing treatments through intelligent connections across the healthcare ecosystem.
- • In this role, you will build strong expertise in clinical trial monitoring, regulatory compliance, and cross-functional collaboration while gaining exposure to diverse therapeutic areas and global study designs. You’ll develop advanced skills in site management, data quality assurance, and stakeholder communication — positioning yourself for long-term growth within IQVIA’s clinical research career pathways.
🎯 Requirements
- • University degree in life science or another scientific discipline, or apprenticeship in healthcare
- • Proven experience as a CRA, Study Coordinator/Nurse, or Clinical Trial Coordinator
- • Strong command of both German and English (written and verbal)
- • Valid Driver’s License Class B
- • Flexibility to travel up to 70% of working time
🏖️ Benefits
- • Home-office setup with company car provided
- • Accident insurance, pension plan, and additional employee benefits
- • Resources and programs to support career growth and therapeutic knowledge development
- • Flexible work schedules supported by leadership
- • Starting monthly gross salary of 4,000 EUR, with potential for overpay based on skills and experience
Skills & Technologies
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About IQVIA Holdings Inc.
IQVIA Holdings Inc. provides advanced analytics, technology solutions, and clinical research services to the life-sciences industry. Formed through the 2016 merger of Quintiles and IMS Health, the company integrates healthcare data, analytics, and domain expertise to help biopharmaceutical and medical-device clients optimize drug development, commercialization, and real-world evidence generation. Its offerings span clinical trial design and execution, real-world insights, commercial strategy, and technology platforms that connect stakeholders across the healthcare ecosystem. Headquartered in Durham, North Carolina, IQVIA operates in more than 100 countries, supporting the development and delivery of therapies to improve patient outcomes worldwide.
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