Unblinded CRA based in Austria
Posted 11 days ago
Who can apply
Austria only
Salary
Not disclosed
Level
Mid level
Full-time
Timezone
UTC +1
About the role
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
If you are looking to build your clinical monitoring career within a high-impact and supportive environment, we encourage you to apply and grow with us.
Learn more about our EEO & Accommodations request here.
Originally posted on Himalayas
Skills mentioned
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About Fortrea
Listing details & historyShowHide
- Employer posted
- 14 Oct 2026
- Last confirmed open
- Not yet confirmed
- Source
- Job board
- Degree
- Degree or equivalent experience
- “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 regula”
- Visa
- Not stated
- “Join a sponsor-dedicated model supporting cutting-edge clinical trials in DACH.”
- Timezone
- Not stated
- Languages
- German
- Location evidence
- “Remote — Austria”
Details are read from the listing text. They are not a guarantee of work authorization; confirm with the employer.
History
- 14 Oct · Added to Remotavia