Study Coordinator

About Pratia Bulgaria

Pratia Bulgaria is part of Pratia, a global clinical research site network. We conduct clinical trials in collaboration with leading pharmaceutical, biotechnology, and CRO companies, helping to advance innovative treatments and improve patient care.

Our team works in a professional and supportive environment, providing opportunities to learn, grow, and contribute to meaningful medical research.

As our clinical trials site in Dobrich continues to grow, we are actively seeking an enthusiastic, English-speaking Study Coordinator to join our dynamic team on-site in Dobrich for a long-term opportunity. We'd love to hear from you if you're driven, detail-oriented, and ready to make an impact in the field of clinical research!

Why Join Us?

Be part of an innovative field: Play a key role in advancing clinical trials and contribute to medical progress.

Work with a supportive team: Collaborate with skilled professionals in a positive, team-driven environment.

Professional Growth: Benefit from comprehensive training and continuous learning opportunities.

Work-life balance: Enjoy a healthy balance between your professional and personal life.

Competitive Salary: We offer an attractive remuneration package.

What We’re Looking For

We’re looking for a self-motivated, curious, and proactive individual who can start as soon as possible and is interested in developing a long-term career in clinical research in our clinical site in Plovdiv, Bulgaria.

Key Requirements

Fluent English (written and spoken);

Strong computer literacy;

Excellent communication and organizational skills;

Team player with a positive and friendly attitude;

Eager to learn and develop new skills;

Demonstrates loyalty, responsibility, and attention to detail;

Ability to meet deadlines and follow established standards;

Willingness to work on-site in Dobrich.

Your Responsibilities

Serve as the main point of contact for partners, colleagues, and patients;

Maintain and organize office documentation;

Input and manage data in electronic databases;

Translate study-related documents;

Provide support to medical staff to ensure smooth workflow;

Ensure timely execution of tasks and adherence to project timelines.

How to Apply

Please submit your CV along with a recent photo.

Only shortlisted candidates will be contacted.

Take the next step in your career with us and make a difference in the world of clinical research!

Rest assured, all personal data shared with us is handled with strict confidentiality, in compliance with the Personal Data Protection Law.