Clinical Intern

    Location: Bucharest, Romania

    Job Type: Full Time

    Salary: 2,200 – 3,000 RON/month

    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.

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