Clinical Research Associate Job at ICON, Austria | Life Sciences | Apply Now
If you are a clinical trial professional or an experienced Study Coordinator looking to advance into international monitoring, this position at ICON plc is an exceptional find. Located in the pharmaceutical hub of Vienna, Austria, this hybrid role allows you to combine remote data review with critical on-site investigator clinic management. For compliance-focused professionals searching for a high-impact Clinical Research Associate Job, this position offers end-to-end site management ownership, data validation auditing, and regulatory trial monitoring. It serves as an elite operational milestone for a long-term ICON career and stands out as a premier choices for anyone tracking a high-growth Life Sciences Job within Europe’s clinical trials sector.
About The Company
ICON plc is a world-leading global Contract Research Organization (CRO) and healthcare intelligence powerhouse driven by a unified mission to accelerate the development of innovative drugs and medical devices. Headquartered in Dublin, Ireland, with a massive operational footprint across Europe, ICON manages centralized laboratory networks and clinical testing footprints spanning multiple continents.
This specific role sits within ICON Strategic Solutions, operating under a Functional Service Provider (FSP) framework. In this highly collaborative model, you are deployed directly into a single, top-tier global pharmaceutical sponsor’s pipeline. This unique infrastructure grants you the ultimate benefit of focusing deeply on the sponsor’s specific protocols and cross-therapeutic compounds, backed by the comprehensive corporate benefits, training platforms, and administrative stability of ICON.
Key Responsibilities
As a CRA II focusing on study start-up and monitoring activities in Austria, you will serve as the primary point of contact between investigational sites and the sponsor, ensuring all medical data streams are executed in total alignment with international regulations.
Your core monitoring, data validation, and site-support duties include:
- Full-Cycle Site Monitoring: Conducting all essential site visit phases—including Site Qualification (SQV), Site Initiation (SIV), Routine Interim Monitoring (IMV), and Close-Out Visits (COV)—across Austria to advance this Clinical Research Associate Job.
- ICH-GCP Compliance Auditing: Evaluating the quality and integrity of study site practices to ensure absolute compliance with study protocols, corporate SOPs, and international ICH-GCP guidelines.
- Patient Safety Oversight: Reviewing clinical records to monitor patient safety, ensuring the accurate tracking, documentation, and timely reporting of adverse events.
- Data Stream Management: Performing detailed data reviews, electronic case report form (eCRF) auditing, and driving rapid resolution of data queries to maintain high-quality data.
- Dossier & Documentation Support: Contributing to the preparation and review of critical study documentation, including protocol amendments, site files, and clinical study reports for this Life Sciences Job.
- Investigator Partnerships: Collaborating closely with regional principal investigators and medical site staff to facilitate smooth study conduct, manage expectations, and resolve ongoing project bottlenecks.
Qualifications & Profile Requirements For Clinical Research Associate Job
This corporate vacancy is systematically tailored for analytical, bilingual communicators who possess the technical confidence to work independently in a fast-paced environment.
- Required Academic & Experience Criteria:
- Educational Foundation: A formal Bachelor’s degree in a scientific or healthcare-related field.
- Industry Track Record: A minimum of 1 year of experience in the clinical research field (such as a Study Coordinator, Clinical Trial Assistant, or a similar clinical operations capacity) to launch an ICON career.
- Linguistic Mastery: Absolute fluency in both German and English (written and verbal) is required to manage regional site documentation and global team communications.
- Travel Flexibility: Willingness and ability to travel as required to clinical sites across Austria (approximately 60% field travel).
- Technical Skills & Competencies:
- In-depth knowledge of clinical trial processes, local Austrian regulations, and international ICH-GCP guidelines.
- Strong organizational habits, high attention to detail, and a commitment to accuracy in documentation.
- Proficient computer capability navigating standard productivity software and electronic data capture portals.
In short, the Clinical Research Associate position at ICON is a definitive route to transitioning your foundational study coordination or life sciences background into a globally recognized clinical operations asset. Securing this appointment allows you to move past localized logistics and take direct operational charge of the site relationships, patient safety metrics, and data query pathways that drive breakthrough therapies into global medical markets. If you reside in Austria, speak fluent German and English, and meet the 1-year clinical research threshold, apply today to secure this premier Clinical Research Associate Job, launch a highly rewarding ICON career, and lock in this outstanding Life Sciences Job.
