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Teva Sr Mgr Biostatistics Mexico, Guanajuato 723842428
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How you’ll spend your day
- 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
Your experience and qualifications
- Ph.D./MS in Statistics/Biostatistics (or related field)
- MS with a minimum of 10 years of related experience; PhD with a minimum of 6 years of related experience
- Proficiency in statistical programming languages (e.g., R, SAS) and experience with data visualization tools
- Regression modelling, Simulation, Adaptive trial designs, Bayesian statistics, Experimental design
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