A Principal Biostatistician is responsible for independently planning and managing project deliverables and study-level analysis and reporting activities and for providing statistical support for clinical trials.
Project Management Responsibilities:
Standard Operating Procedures (SOPs):
The ideal candidate should have an advanced degree (MS or PhD) in Statistics or a closely related field, with a minimum of 5 (PhD) or 7 (MS) years of experience in pharmaceutical development and SAS programming for statistical analysis. Candidate must have experience in clinical trial design and must comply with regulatory requirements. Excellent oral and written communication skills, organizational skills, and attention to detail are required.
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