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Sr. Biostatistician
Ref No.: 17-14967
Location: San Francisco, California
Provides statistical input into Phase I - IV clinical trial development. Designs and analyzes clinical trials. Maintains the statistical and analytical integrity of clinical trials analyzed. Participates in writing statistical sections of protocols, preparing statistical analysis plans, preparing data deliverables for clinical study reports, and interpreting statistical results for clinical study reports. Acts as the lead statistician on clinical research projects and help with SAS programming. Provides statistical expertise for study design of clinical trial protocols. Writes statistical methods section of the study protocol. Develops statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed. Performs all analyses defined in the statistical analysis plan as well as any post-hoc analyses and relevant exploratory analyses of clinical trial data. Performs validation of statistical results. Provides input to key sections of clinical study reports and various regulatory documents.

A minimum of 8 years experience in the Pharmaceutical, Medical Products industry, pharmaceutical product development or pharmaceutical formulations development is required. Excellent analytical skills with the ability to process scientific and medical data is required. Must be able to work independently and in teams. Must have a thorough knowledge of SAS software. Must have demonstrated problem solving abilities. Strong organizational skills are required. Strong written and verbal communication skills are required. Must have demonstrated good interpersonal skills. Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).