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Clinical trial assistant
Flemish BrabantOn site36 hours/week3-6months
Temporary reinforcement for a team within a medical department.
- The assignment focuses on clinical studies and patient contact.
What you do
- Organization, practical follow-up, coordination, and administrative processing of clinical studies.
- Administering questionnaires to patients included in the study.
- Collecting data for clinical studies, managing the database, and performing necessary analyses.
- Participating in multidisciplinary consultations, as well as consultations with external companies.
- Good collaboration with other study staff, medical staff, internal, and external contacts is essential.
- Working on a fixed schedule without weekend or night activities, but a certain degree of flexibility in hours is possible in mutual consultation.
What they ask
- Bachelor's or Master's degree in nursing or a Master's in biomedical sciences.
- Passion for clinical scientific research and a broad interest in the follow-up of clinical studies.
- Good communication and social skills, and team-oriented.
- Good knowledge of English and French.
- Excellent administrative skills and good knowledge of MS Office (Excel, Word, and PowerPoint).
- Ability to work autonomously and punctually with a sense of initiative.
- Organizational talent and excellent problem-solving ability.
- Stress-resistant and flexible.
- A clear criminal record extract (model 596-2) is necessary if you come into contact with minors in this position.
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