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Clinical Trials Office Administrator — Varna, On-Site
Support clinical trial administration in Varna by organizing documentation, coordinating study activities, and assisting Pratia’s clinical research team. Maintain accurate records and help uphold quality and compliance standards.
विवरण
- Manage and organize clinical trial documentation
- Keep records complete, accurate, and current
- Provide day-to-day administrative support to the clinical research team
- Assist with study coordination and team organization
- Communicate with investigators, patients, and external partners as required
- Use internal systems for document and data management
- Help coordinate office operations and clinical trial activities
- Contribute to strong quality and compliance practices
आवश्यकताएँ
- Strong organizational skills and careful attention to detail
- Ability to manage multiple tasks and changing priorities
- Clear communication skills and a collaborative approach
- Fluent written and spoken English
- Working knowledge of Microsoft Office
- Proactive, dependable, and willing to learn
- Interest in building a career in clinical research
- Medical or clinical documentation experience is helpful but not required
- Motivation, organization, attention to detail, and eagerness to learn
- Submit a CV in English
लाभ
- Join a supportive team with experienced colleagues
- Receive professional training and develop clinical research knowledge
- Gain experience in an international clinical research setting
- Access opportunities for professional and personal development
- Work in a dynamic environment where contributions are valued
- Build a career with Pratia and Humaneva Group
- Receive competitive compensation and benefits
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