Posted:3 weeks ago|
Platform:
Hybrid
Full Time
Primarily works at the Product/Program Level
Provide input for budget planning
Manage and Deliver assignments with quality and within timelines
Possible to have direct reports; Possible to oversee contingent workers and/or vendors; likely to provide training to others; Analyzes needs to manage resources
Responsible for statistical aspect of study designs and data analyses for clinical studies
Provides study design input and consultation for clinical endpoint assessments and sample size planning
Prepares, or oversees the preparation of statistical sections of clinical protocols in collaboration with key stakeholders, as deemed necessary
Writes, or oversees the writing of, statistical analysis plans
Conducts, or oversees the conduct of, analyses to support clinical study reports, abstracts, manuscripts, and other documents to support the marketing of Teva products
Leads the conduct of analyses and document preparation to support global regulatory submissions, including briefing packages, integrated analyses, and regulatory responses.
Collaborates with outsourcing partners and oversees conduct of statistical aspects of outsourced studies, as appropriate
Proactively assesses and identifies processes that require improvement
Participates in department initiatives to further the effectiveness of global statistics
Implements innovative and cutting-edge clinical trial design, methodology and analysis
Ph.D./MS in Statistics/Biostatistics (or related field)
Teva Pharmaceuticals
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