
Clinical Research Associate
2 weeks ago
This role offers a chance to develop key skills, work alongside experienced professionals, and build a strong foundation for your future in clinical research.
- Accurately enter and verify clinical data from Case Report Forms (CRFs) into study databases following established guidelines
- Perform quality control checks to ensure data integrity and compliance with regulatory standards
- Assist in database testing, documentation preparation, and processing of clinical data for multiple projects
- Support User Access Management for Electronic Data Capture (EDC) systems and maintain related documentation
- Master's degree in life sciences background
- Proficient PC skills, including Excel and Word
- Basic knowledge of Clinical Data Management
- Analytical skills and attention to detail
- Excellent communication skills, oral and written
- Familiarity with ICH Guidelines and GCP
- Hands-on experience in clinical data management within a regulated environment
- In-depth understanding of industry standards and regulations
- Exposure to project management and teamwork across global clinical research teams
- Development of strong analytical, communication, and technical skills using industry-leading tools and systems
We are an equal opportunities employer.
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