The opportunity
The Senior Manager Clinical Statistician position is for a skilled statistician with training and experience in drug development and non-clinical research. He or she is expected to provide statistical support to clinical studies or programs within Teva Global R&D. The support includes, but not limited to, stake holder engagement, strategic thinking & problem solving, planning, study designs, data analyses, and regulatory interactions. He or she is expected to have extensive knowledge about statistical principles and appropriate software and tools to perform his or her tasks. A Senior Manager Non-Clinical Statistician should be a strong individual contributor and demonstrates leadership qualities. They must have excellent written and oral communication skills and demonstrate the ability to successfully working in a global environment.
This is a remote position
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 non-clinical projects
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
