Clinical Intern - Romania

At Fortrea, we believe early talent is the heartbeat of innovation. Our Early Careers program is more than an internship —it’s a launchpad for your future.

As an Intern , you’ll join a global team where curiosity, motivation, and fresh ideas are celebrated. You’ll work on meaningful projects, learn from experienced professionals, and see firsthand how clinical research and healthcare innovation change lives.

We don’t expect you to know it all. What matters most is your potential, your drive to learn, and your willingness to grow. With hands-on experience, mentorship, and structured development, we’ll help you build the skills and confidence to succeed.

Your journey to pioneering tomorrow’s breakthroughs starts here.

Job Overview:

The Clinical Research Intern will support the following departments—Clinical Operations, the planning, execution, and oversight of clinical trials. This internship provides hands-on exposure to operational, analytical, or data-focused aspects of clinical research. It is designed for students or recent graduates interested in clinical development, trial management, or data-driven research.

Candidates must be based in Bucharest area.

Summary of Responsibilities:

Assisting in the preparation, review, and maintenance of clinical trial documents.

Supporting communication and coordination with clinical trial sites.

Participating in data entry, tracking, and quality control activities.

Helping prepare materials for regulatory submissions and ensuring compliance with applicable guidelines.

Monitoring study progress, including enrollment tracking and visit schedules.

Conducting literature reviews and summarizing findings relevant to ongoing studies.

Performing administrative tasks to support the assigned team.

Supporting internal audits or inspections readiness activities

Qualifications (Minimum Required):

MUST HAVE : c urrently enrolled in or recently graduated from a degree program in life sciences, public health, pharmacy, or another related field.

Demonstrated interest in clinical research, trial operations, statistical programming, or data management.

Strong organizational and time-management skills.

Detail-oriented with a commitment to high-quality work.

Effective communication skills and ability to work collaboratively.

Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

Ability to handle confidential information with discretion.

Preferred Skills

Familiarity with Good Clinical Practice (GCP) and clinical trial processes.

Experience with CTMS, EDC platforms, or statistical software (e.g., SAS, R) is a plus.

Physical Requirements:

Frequently stationary for 8 hours per day .

Ability to access and use a variety of computer software developed both in-house and off-the shelf.

Regular and consistent attendance.

Varied hours may be required.

Learn more about our EEO & Accommodations request here .