Location: Bucharest, Romania
Job Type: Full Time
Salary: 300€ to 800€ per month
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.
Full-time and part-time internships available.
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: currently 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.