Unblinded CRA based in Austria

Fortrea; Wien; Hybrid; EUR 48,000 - 64,000; Full time

Benefits offered by this job

Structured onboarding

Flexible working model

Global career growth

Inclusive culture

Wellbeing initiatives

Job summary

Fortrea in Austria is seeking an unblinded Clinical Research Associate (CRA I or CRA II) to support unblinded study activities within a sponsor-dedicated environment. You will contribute to high-quality clinical research delivery while gaining exposure to unblinded processes in a collaborative global setting.

The role offers structured onboarding, flexible working arrangements, and opportunities for professional growth in clinical operations across the DACH region, with travel within

Qualifications

• Bachelor’s degree in Life Sciences or related field (or equivalent experience).
• 1+ year of clinical research monitoring experience as CRA.
• Understanding of ICH-GCP and trial processes.
• Interest in unblinded study conduct and Investigational Product management.
• Fluency in German and English.
• Willingness to travel within Austria or Germany.
• Strong organizational skills with attention to detail.

Responsibilities

• Perform unblinded monitoring in line with ICH-GCP and regulations.
• Ensure protocol compliance, data integrity, and patient safety at sites.
• Maintain study documents, eTMF, and regulatory files.
• Engage site staff as primary contact for site management (pharmacy only).
• Contribute to audit readiness and inspections at site level.

Skills

Unblinded monitoring

ICH-GCP knowledge

German language

English language

Travel willingness

Attention to detail

Organizational skills

Education

Bachelor’s degree in Life Sciences or related field

Job description

Join a sponsor-dedicated model supporting cutting-edge clinical trials in DACH. As an unblinded Clinical Research Associate (CRA I or CRA II level) , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment.

Key Responsibilities

• You will perform unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product oversight
• You will ensure protocol compliance, data integrity, and patient safety at assigned sites
• You will maintain accurate and complete study documentation, including eTMF and regulatory files
• You will build strong relationships with site staff, acting as the primary point of contact for site management (pharmacy only)
• You could contribute to audit readiness and ensure inspection preparedness at site level

Required Qualifications

• Bachelor’s degree in Life Sciences or related field (or equivalent experience)
• Initial experience in clinical research as a CRA with at least 1 year of monitoring experience
• Understanding of ICH-GCP guidelines and clinical trial processes
• Strong interest and knowledge in unblinded study conduct and Investigational Product management
• Fluency in German and English (written and spoken)
• Willingness to travel within Austria or Germany as required
• Strong organizational skills with attention to detail

What We Offer

• Opportunity to work in a sponsor-dedicated environment on innovative studies
• Structured onboarding and continuous development programs
• Flexible working model supporting work-life balance
• Access to global career growth opportunities within clinical operations
• Inclusive and collaborative culture with employee resource groups and wellbeing initiatives

Learn more about our EEO & Accommodations request here.