Unblinded CRA based in Austria

Fortrea; United States; Remote; USD 58,000 - 78,000; Full time

Benefits offered by this job

Sponsor-dedicated environment

Structured onboarding

Flexible working model

Global career growth

Job summary

Fortrea is seeking an unblinded Clinical Research Associate (CRA I or CRA II) to support cutting-edge clinical trials in the DACH region. You will conduct unblinded monitoring in compliance with ICH‑GCP, manage Investigational Product oversight, and partner with site staff to ensure data integrity and patient safety.

The role requires a life sciences degree, 1+ year CRA monitoring experience, German and English fluency, and willingness to travel within Austria or Germany.

Qualifications

• Bachelor’s degree in Life Sciences or related field (or equivalent experience).
• 1+ year of monitoring experience in clinical research.
• Understanding of ICH-GCP guidelines and trial processes.
• Interest 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.

Responsibilities

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

Skills

CRA monitoring

ICH-GCP

German language

English language

Attention to detail

Travel willingness

Education

Bachelor's degree in Life Sciences

Job description

Location: Austria

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