Clinical Trials Assistant, Belgium
On-site · Brussels, Brussels Capital, Belgium
Job Summary
Clinical Trials Assistant in Belgium supports daily administrative activities with Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams to ensure accurate TMF delivery. Responsibilities include updating and maintaining clinical documents and systems, preparing, handling, distributing, filing, and archiving clinical documentation and reports, reviewing study files for completeness, assisting with Clinical Trial Supplies and material tracking, supporting the management of Case Report Forms and data flow, and serving as a central contact for project communications. MAY accompany CRAs on site visits for monitoring duties after training, and requires proficiency in English, Dutch, and French and knowledge of GCP/ICH guidelines.
Required Qualifications
- High School Diploma or equivalent
- Working knowledge of Microsoft Word, Excel and PowerPoint
- Written and verbal communication skills in English, Dutch and French
- Effective time management and organizational skills
- Ability to establish and maintain working relationships with coworkers, managers, and clients
- Awareness of applicable clinical research regulatory requirements (GCP, ICH) as provided in company training
- Knowledge of applicable protocol requirements as provided in company training
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