- Develop clinical trial strategies to support product registration and marketing.
- Provide medical and scientific input to product development (from first-in-man trials up to reimbursement and market access)
- Provide scientific and methodological expertise in the development of clinical research programmes
- Act as a scientific source particularly to the clinical research department (protocol and CRF writing, handling of statistical data and sample size calculation)
- Manage scientifically and operationally the clinical projects to achieve the clinical program goals and objectives
- Manage budget and timelines for own projects
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