• Act as a Global Project Statistician for complex/high profile projects • Responsible for all statistical aspects of a clinical development plan and interactions with regulatory authorities • Coordinate biometrics activities for global projects liaising with Japan and US • Train and coach biostatisticians (but not as line manager)
Functie eisen
• Academic qualification in Statistics • Advanced knowledge of statistical methods for clinical research and current industry practices • Advanced knowledge of base SAS & SAS/STAT programming • Very good understanding of clinical development processes and ability to see the overall picture • At least 8 years of experience in applying statistical methods in biomedical research • Pharmaceutical or CRO industry experience • Very good personal skills in communication, teamwork, etc.
Bedrijfsprofiel
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