Study Coordinator

About Pratia

Pratia, part of Humaneva Group, is one of Europe's leading clinical research networks, operating more than 90 research sites across 7 countries. We partner with leading pharmaceutical, biotechnology, and CRO organizations to help bring innovative treatments to patients faster.

The Opportunity

We are looking for a proactive and detail-oriented Study Coordinatorto join our growing clinical research team.

In this role, you will support the day-to-day coordination of clinical trials, working closely with investigators, patients, sponsors, and site staff to ensure studies are conducted efficiently and according to quality standards.

What You'll Do

• Support the coordination of clinical trial activities.
• Maintain study documentation and site records.
• Manage data entry and updates in electronic systems.
• Communicate with patients, investigators, and external partners.
• Assist with study-related documentation and translations.
• Support investigators and medical staff in daily site activities.

What We're Looking For

• Fluent English, written and spoken.
• Strong computer literacy and MS Office skills.
• Excellent organizational and communication skills.
• Attention to detail and ability to meet deadlines.
• Positive, proactive, and team-oriented attitude.
• Interest in building a career in clinical research.

What We Offer

• Competitive salary package.
• Performance-based bonus.
• Meal vouchers.
• Additional health insurance.
• Comprehensive training and onboarding.
• Professional development opportunities.
• Supportive and collaborative team environment.
• Career growth within Pratia and Humaneva Group.

Why Join Us?

This is a great opportunity to build a long-term career in the rapidly growing field of clinical research while contributing to innovative studies that help improve patients' lives.

Apply Now

If you're ready to take the next step in your career, we'd love to hear from you. Please submit your CV in English.

Only shortlisted candidates will be contacted.