Clinical Research
1. Clinical Trial Assistant
The CTA is member of the clinical project team and supports the Project Manager and CRA in-house. The CTA is responsible for the administrative part of the clinical trials: correspondence, set-up documents, filing and archiving and additional tasks within the clinical project.
Requirements
- Master Biomedical Sciences, Bachelor medical management assistant
- Microsoft Word, Excel, Powerpoint
- Good communication skills
- Team spirit
- Well organized
- Fluently Dutch, French & English
- Dynamic personality
2. Clinical Research Associate
The CRA is the go-between the investigator and the pharmaceutical company; ensuring that the clinical study is conducted according the guidelines. He/she is monitoring the collected data in the patients' files and the medical records, informing the investigator of incorrect or missing data.
Requirements
- Scientific background
- Master’s degree/ PhD in scientific area
- Accuracy
- Flexibility
- Good communication & organization skills
- Fluently Dutch, French & English
3. Clinical Data Management
The data manager handles the collected data, centralizes, verifies and validates the information in the clinical database for statistical processing. A job requiring precision, patience and stress-resistance.
Requirements
- Scientific background
- Master’s degree/ PhD in scientific area (Drug Development/ Biomedical Sciences)
- Accuracy
- Flexibility
- Good communication & organization skills
- Fluently Dutch & English
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