- Location
- Bucharest, Romania
- Workplace
- Hybrid
- Type
- Full-time
- Source
- Workday
Description
Are you detail-oriented and passionate about supporting clinical research operations?
If so, join our team in Bucharest as a Clinical Trial Coordinator, where you’ll play a key role in supporting clinical studies. This is a sponsor-dedicated, office-based position (hybrid model) offering meaningful exposure to global clinical development.
Key Responsibilities
You will:
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
Experience in clinical research preferred
Strong proficiency in Microsoft Office (Excel, Outlook, Word, PowerPoint).
High affinity for electronic systems and document management tools.
Fluent in Romanian 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 Bucharest 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.
