The Associate Director of Biostatistics will perform highly scientific statistical functions in support of the company's Global Medicines Development and Affairs (GMDA) area with minimal guidance and mentoring on new and complex issues. He/She will serve biostats lead role on assigned projects including Phase 3b/4 clinical studies, real world evidence (RWE) studies, market access and reimbursement, and other post-approval and medical affairs activities.
He/She will complete assigned work in a resourceful, self-sufficient manner and create alternative approaches to achieve desired results if needed. In addition, the Associate Director is capable of independent strategic and technical contributions. Skill in project and personnel oversight may also be required. He/she should possess a good knowledge of related disciplines while performing Biostatistics activities with a drug developer mindset.
Key Responsibilities
The Associate Director of Biostatistics:
Minimum Qualifications
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