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Clinical Project Manager
Brussel
Job description
- Overall management of clinical studies (deadlines, budget, recruitment, SAE, etc.)
- Organise investigator meetings
- Coordinate CRO selection
- Vendors management
- Support the preparation of Clinical Trial Protocols
- Prepare annual safety reports
- Ensure the development of safety monitoring plans
- Organise clinical meetings (manage agenda and minutes)
Benefits
- 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
Have you got what it takes?
Apply- Bachelor or Master's degree in a scientific field
- Minimum 5 years of experience in clinical research
- Previous experience in Project Management preferred
- Fluency in English is a must, French preferred, Dutch an asset
Reference number: 31730
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