Clinical Trial Assistant
Region
Flemish Brabant
Reference
16150
Responsibilities of the Clinical Trial Assistant
- Administers, maintains and coordinates the logistical aspects of clinical trials according to GCP (Good Clinical Practice) and relevant SOP’s
- Acts as a pivotal point of contact for the clinical trial team
- Supports the clinical trial team in various administrative tasks
- Prepares, translates, reviews and files documentation for clinical trials
- Helps process improvements initiatives, including developing SOP’s
- Provides agenda, minutes and action points for meetings
- Supports processes related to setting up and tracking of trainings
- Follows up on contracts, letters of intent, POs, invoices
Profile of the Clinical Trial Assistant
- Bachelor’s degree in life science or related field
- At least 2 years of experience in clinical environment
- Excellent verbal and written communication skills
- Sound knowledge of Windows and MS Office (word, excel, access, powerpoint)
- Flexible and proactive approach
- Fluency in English (spoken/written), Dutch and/or French
Offer for the Clinical Trial Assistant
- Challenging projects based on your interests and skills
- Personal follow-up and clear, transparent communication both before and after commencement of employment
- Possibility to follow extra training
- Inspiring network events and legendary after work drinks
- Strong network of industry leading clients
- Expertise within IT, Engineering and Life Sciences
- A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employees
