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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