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Clinical Studies Assistant

Flemish BrabantHybrid36 hours/week<3months

What you will do.

  • Collect data by participating in the clinical evaluation of study participants.
  • Enter, correctly store, and organize data.
  • Collaborate with the data manager for data quality control.
  • Contribute to the processing and analysis of clinical endpoints, in collaboration with other team members.

Profile

  • Bachelor's degree in biomedical sciences.
  • Demonstrated experience with biomarker research in neurodegeneration.
  • Perfectly bilingual in Dutch and French, and proficient in English.
  • Eager to learn and willing to delve into clinical research.
  • Enjoys working with human study participants and is willing to apply conventional as well as new methods to evaluate cognition and function.
  • Experience or strong affinity with electronic data management and data quality control.
  • Knowledge of at least one programming language (e.g., R or Python).
  • Knowledge of regulations regarding the processing of personal data (incl. GDPR) or willingness to quickly familiarize yourself with them.
  • Passion for scientific research.
  • Proficient with digital platforms and tools.
  • Work accurately, reliably, and punctually.
  • Contact-oriented and communicative.
  • Easily integrate into a multidisciplinary team.
  • Work independently, be driven, and take initiative.
  • Be open to feedback and take initiative to keep knowledge up to date and follow new developments.

How to apply

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