AbbVie
10,000+ employees
Founded 2013
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
Pharmaceuticals • Biotechnology • Healthcare Insurance
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
Clinical Research Associate
🔥 0 minutes ago
🗣️🇩🇪 German Required
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AbbVie
10,000+ employees
Founded 2013
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
Pharmaceuticals • Biotechnology • Healthcare Insurance
AbbVie is a global pharmaceutical company that discovers and delivers innovative medicines and solutions to enhance lives. With a focus on addressing the world's toughest health challenges, AbbVie operates in over 175 countries, providing a wide range of products across areas like immunology, oncology, neuroscience, and aesthetics. Committed to scientific innovation, AbbVie invests heavily in research and development, aiming to produce first-in-class medicines. The company also emphasizes workplace diversity, sustainability, and patient support initiatives, ensuring positive impact for both its patients and the broader community.
📋 Description
• Supervision of and continuous communication with investigational sites in the implementation of global clinical trials • Site management and monitoring activities such as on-site and remote site initiations • Monitoring and close-out visits for Phase I–IV clinical trials • Independent management of investigational sites; training study physicians and site staff prior to site activation • Preparation and updating of study-related documents • Support in site selection, collection of all relevant study documents, and preparation of submissions in CTIS • Ensuring compliance with all internal and external requirements as well as ICH-GCP guidelines • Documentation of visits and protocol deviations during the study
🎯 Requirements
• Degree in a natural science or health science field, or comparable relevant training • Experience in clinical trials • Organizational talent with an outgoing personality and the ability to motivate others • High degree of flexibility, team orientation, strong communication skills, and assertiveness • Willingness to travel (average 5 days/month) • Very good English and German skills • Very good MS Office skills
🏖️ Benefits
• Promote diversity • Develop potentials and strengths • Turn ideas into reality and seize opportunities
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