Clinical Trial Assistant
View: 115
Update day: 16-11-2025
Location: Vilvoorde Flemish Brabant
Category: Executive management
Industry:
Job type: Voltijds, Deeltijds, Vaste Jobs
Job content
Purpose:
You will provide support (administrative, logistic and document management) in the preparation and execution of all study related activities within agreed timelines.
Major Accountabilities:
- Specialists responsible for administrative management of trials
- Responsible for the preparation, tracking, processing of all study related documentation and material
- Manages logistics and document exchange between clinical sites and our company
- Updates clinical study management systems
- Works in continuous collaboration with other associates/team members
- Applies company policies and procedures to resolve routine issues.
- Contacts are primarily with immediate supervisor and other personnel in department or group
- Works on problems of routine scope. Follows established policies and procedures.
- Normally receives detailed instructions on all work
Clinical Trial Supplies:
- Assists local trial team with the creation, ordering, and mailing of any study tools including recruitment materials as well as newsletters, email communications, faxes, etc.
- Supports local trial team with ordering/tracking/mailing of any necessary trials supplies including the regulatory binder, lab kits.
- Support the CSM with the coordination of internal and external suppliers, including customs, to ensure import of all clinical trial supplies (including drug supply)
- Coordinate shipment of clinical trial supplies to local sites
- Co-ordinate relabeling of IMP at warehouse when needed.
Finance:
- Track, process and release payments to vendors in collaboration with local study team and finance.
Dienstverband: Voltijds, Deeltijds, Vaste Jobs
Loon: Vanaf €2.100,00 per maand
Aanvullende betalingen:
- 13e maand
- Bonusregeling
- Vakantiegeld
Voordelen:
- Ecocheques
- Een gsm voor professioneel gebruik
- Eindejaarsgeschenk
- elektronische maaltijdcheques
- Flexibele werkuren
- Hospitalisatieverzekering
- Internetvergoeding
- Laptop van de zaak
- Pensioensparen
- Thuiswerkopties
Werkschema:
- Dagdienst
- ma-vr
Opleiding:
- Bachelor (Aanbevolen)
Ervaring:
- clinical research: 1 jaar (Aanbevolen)
Taal:
- Nederlands en Engels (Aanbevolen)
Deadline: 31-12-2025
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