Clinical Research Associate (m/f/d)
Confirmed on the employer's own hiring board on Nov 1, 2026. First seen by Alion on Oct 28, 2026. AbbVie scores B on the Alion truth index.
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
You are an excellent organizer and have outstanding social skills and persuasive ability? Then this key role as a Clinical Research Associate is exactly right for you!
As a research-based biopharmaceutical company, AbbVie is one of the most successful companies in the industry internationally and a top employer in Austria. We are currently looking for active support for the Clinical Research Team at our Vienna location. Motivated and experienced CRAs are very welcome in this great team!
Clinical Research Associate (m/f/d)
Realize your interests in a fulfilling career and actively change patients’ lives for the better!
Your responsibilities:
- Supporting and maintaining continuous communication with study 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 clinical trials in Phases I-IV, independent management of sites, and training of study physicians and site staff before site activation, as well as during the study.
- Preparing and updating study-related documents, as well as supporting, training, and motivating site personnel; revising patient informed consent forms.
- Study start-up activities, such as country and site feasibility in coordination with the medical department, support in site selection, obtaining all relevant study documents, preparing submissions in CTIS, and creating, submitting, and tracking applications to national authorities and ethics committees.
- Compliance: ensuring adherence to all internal and external requirements, as well as ICH-GCP guidelines, legal regulations, study protocols, and SOPs.
- Support administrative tasks such as updating study management systems, documenting visits and protocol deviations during the study, or submissions in CTIS.
Your experience and skills:
- Degree in natural sciences or health sciences, or comparable relevant training.
- Experience in the clinical research field.
- Strong organizational skills, an open personality, and the ability to motivate others.
- High degree of flexibility, teamwork, communication skills, and assertiveness.
- Enjoyment of traveling (average 5 days/month).
- Proficiency in English and German.
- Very good MS Office skills.
As an employer, we value diversity and support people in developing their potential and strengths, realizing their ideas and seizing opportunities. The job advertisement is aimed equally at all people, regardless of age, skin color, religion, gender, sexual orientation or origin. For legal reasons, we are obliged to point out that the minimum salary for this position under the collective agreement is € 2,879.00 gross per month. However, our attractive salary packages are based on current market salaries and are therefore significantly higher than the stated minimum salary.
AbbVie setzt sich für Chancengleichheit ein und verpflichtet sich, mit Integrität zu arbeiten, Innovationen voranzutreiben, Leben zu verändern und unserer Gemeinschaft zu dienen. Chancengleichheit bei Arbeitgeber/Veteranen/Behinderten.