Vienna Clinical Research Associate — Global Trials

AbbVie Inc.; Wien; On-site; EUR 29,000 - 35,000; Full time

Job summary

AbbVie Inc. in Vienna is seeking a Clinical Research Associate (m/f/d). Realize your interests in a fulfilling career and actively change patients’ lives for the better. The role focuses on site management, monitoring, and study start-up activities across Phases I–IV.

You will support communication with study sites, train site personnel, and ensure adherence to ICH-GCP guidelines, regulations and protocols. Occasional travel is expected, averaging about 5 days per month.

Qualifications

• Degree in natural sciences or health sciences or comparable training.
• Experience in the clinical research field.
• Strong organizational skills 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.

Responsibilities

• Supporting and maintaining continuous communication with study sites in the implementation of global clinical trials.
• Site management and monitoring activities, including on-site and remote site initiations, monitoring and close-out visits for Phases I–IV, independent site management, and training of site staff.
• Preparing and updating study-related documents and supporting site personnel; revising patient informed consent forms.
• Study start-up activities including country/site feasibility, site selection support, CTIS submissions, and authority/ethics submissions.
• Ensure compliance with ICH-GCP guidelines, legal regulations, study protocols and SOPs.
• Support administrative tasks such as updating study management systems and documenting visits and protocol deviations.

Skills

Strong organizational skills

English

German

Teamwork

Communication skills

Travel willingness

Education

Degree in natural sciences or health sciences

Tools

MS Office

Job description

AbbVie Inc. in Vienna is seeking a Clinical Research Associate (m/f/d). Realize your interests in a fulfilling career and actively change patients’ lives for the better. The role focuses on site management, monitoring, and study start-up activities across Phases I–IV.

You will support communication with study sites, train site personnel, and ensure adherence to ICH-GCP guidelines, regulations and protocols. Occasional travel is expected, averaging about 5 days per month.