About the role
Are you detail-oriented and passionate about supporting clinical research operations? Join our team as an FSP Clinical Project Coordinator , where you’ll play a key role in enabling regulatory workflows across clinical studies. This is a sponsor-dedicated, office-based position in Vienna offering meaningful exposure to global clinical development.
Please note this role is for upcoming future opportunities that may arise at Fortrea.
Key Responsibilities
You will:
- Coordinate administrative tasks related to regulatory submissions.
- Maintain trackers, logs, and documentation in compliance with internal SOPs and external regulations.
- Support the preparation and review of study-related documentation.
- Liaise with internal teams to ensure timely updates and data accuracy.
- Assist in scheduling meetings, managing email communications, and organizing project files.
- Monitor timelines and escalate delays or issues to relevant stakeholders.
- Contribute to continuous improvement of administrative processes.
Required Qualifications
- At least 1 year work experience in clinical trial environment
- Some experience in clinical research preferred
- Regulatory administrative background.
- Strong proficiency in Microsoft Office (Excel, Outlook, Word, PowerPoint).
- High affinity for electronic systems and document management tools.
- Fluent in German and English (verbal and written).
- Excellent organizational skills and attention to details.
What We Offer
- A collaborative and inclusive work environment.
- Opportunities for professional development in clinical operations.
- Client-office-based role in Vienna with structured onboarding and training.
- Employee resource groups and wellness programs.
- Competitive compensation and benefits
If you’re ready to contribute to impactful clinical research through precise coordination and support, we encourage you to apply. We welcome applicants from diverse backgrounds and experiences
Learn more about our EEO & Accommodations request here .
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