Careers
Job Description Duties and Responsibilities: - Project management - Manage clients - Statistical data monitoring and central randomization - Statistical analysis - Statistical, integrated reports and manuscripts - Study design, protocol and clinical program development - Statistical support for regulatory submissions Qualifications - M.Sc., MMath. or Ph.D. in Biostatistics or Statistics - At least 3 years Pharmaceutical Industry experience - Experimental design: theory preferably with some healthcare-related research experience - SAS programming, including data manipulations of large clinical datasets - Understanding the principal aspects of clinical research (or the ability to learn them quickly) - Ability to read a clinical research protocol and outline the required statistical analyses - Excellent report writing skills - Quantitative mind - Organized/detail-oriented - Good communication skills - Project management (in-house) and client contact Back to Careers | ||||||
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