Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
$204к-306к/год
$200к$230кмедиана$260к
По похожим ролям (50) ~ $230к/год
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Крутая вакансия
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У роли понятная зона ответственности для руководителя, сильные льготы и работа в известной биотехнологической компании; позиция сочетает влияние на клинические разработки и управление командой.
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Широкая ответственностьАктуальные инструментыСильные льготыВлияние на медицину
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Director, Biostatistics (Biotechnology): Leading statistical strategy and analysis for clinical trials, observational studies, and real-world data investigations with an accent on advanced methods, regulatory interactions, and cross-functional drug development. Focus on directing complex projects, developing statistical analysis plans and data review deliverables, managing biostatistics staff, and implementing innovative study designs.
Location: Boston, Massachusetts, United States. Hybrid option with remote work up to two days per week, or on-site work five days per week with ad hoc flexibility.
Base salary: $204,000–$306,000 per year. The role is also eligible for an annual bonus and annual equity awards.
Company
Vertex is a global biotechnology company that invests in scientific innovation and develops medicines.
What you will do
Direct projects covering multiple clinical trials, observational studies, and real-world data investigations, including presentations to internal senior review boards.
Manage, mentor, and develop direct reports while promoting effective project-team operation and cross-functional collaboration.
Represent Biostatistics on cross-functional teams, set technical and scientific direction, and provide strategic and expert statistical guidance.
Author Statistical Analysis Plans, including table, figure, and listing shells, as well as Cross-functional Data Review plans, Key Reports Memos, and Data Dissemination Plans.
Lead collaboration with statistical programming and other functions to deliver technically sound tables, figures, and listings.
Lead or contribute to regulator, payer, review board, publication, poster, statistical review forum, and departmental working-group activities.
Requirements
Ph.D. or master's degree in Statistics or Biostatistics.
Typically 10 years of experience with a Ph.D., 13 years with a master's degree, or an equivalent combination of education and experience.
Project management and project-team oversight experience.
Expertise with SAS and R statistical software.
Demonstrated expertise in advanced and complex statistical methods used in drug development.
Expert understanding of modern drug discovery and development processes, with a drug developer mindset.
Strong critical thinking, logical problem-solving, written communication, verbal communication, and ability to influence peers and managers.
Ability to collaborate effectively with non-statisticians and explain complex concepts to non-technical audiences.
NDA/MAA experience and direct dealings with United States and European regulators.
Culture & Benefits
Continuous learning and encouragement to stay informed about advances in AI, technology, automation, and industry trends.
Medical, dental, and vision benefits, generous paid time off, and week-long summer and winter company shutdowns.
Educational assistance programs, including student loan repayment.
Commuting subsidy, matching charitable donations, and 401(k).
Hybrid or on-site work flexibility under the Flex @ Vertex Program.
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