• Act as a Local/Global Project Statistician • Contribute to the clinical development plan of the project • Lead all statistical aspects of assigned studies: design planning and reporting • Assist Associate Biostatistics Director in more complex/high profile projects • Interact with peers in Japan and US for assigned projects
Functie eisen
• Academic qualification in Statistics • Sound knowledge of current industry practices related to statistical analysis of clinical data • Advanced knowledge of base SAS & SAS/STAT programming • Good understanding of drug development process and ability to see the overall picture • At least 3 years of experience in applying statistical methods in biomedical research • Pharmaceutical or CRO industry experience • Good personal skills in communication, teamwork, etc.
Bedrijfsprofiel
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