Senior Principal Biostatistician
Agios (agios.com) is a biopharmaceutical company committed to applying our scientific leadership in cellular metabolism to transform the lives of patients with cancer and rare genetic diseases. We are growing rapidly with an active research and discovery pipeline across multiple therapeutic areas. Agios has two approved oncology precision medicines and multiple first-in-class investigational therapies in clinical and/or preclinical development.
Agios is seeking an innovative Senior Principal Biostatistician for our Biostatistics team. Our statisticians lead, develop and implement statistical solutions to support all phases of clinical trials and influence decisions across our oncology and the rare genetic disorder platforms. The successful candidate will function as an independent program statistician across multiple clinical development programs, and will supervise study level statisticians/programmers at CROs.
Agios Statisticians are accountable for all biostatistics study deliverables and manage key trial responsibilities including: statistical design of all phases of trials, authoring of SAPs, and conducting just-in-time analyses and data exploration. The successful candidate must possess the desire and ability to work with study teams up through and including leadership responsibilities as part of our growing, evolving group.
Serve as a statistical and project manager for biostatistics deliverables across assigned clinical development programs
Ensure that clinical development programs (or parts assigned) meet scientific, regulatory, and quality requirements
Oversee outsourced biostatisticians/programmers as needed
Perform trial statistician responsibilities including attendance of study team meetings, authoring SAPs, reviewing CRFs, design of phase 1-3 and PK studies, review of protocols/amendments, conducting exploratory data analyses, and performing just-in-time analyses
Apply innovative statistical approaches to study design, analysis and data exploration methodologies, including Bayesian adaptive methods to dose finding
Plan and track study level activities within programs, including resources; ensure CRO timelines and objectives are met
Help to maintain Agios data standards, within and across programs (e.g. standardization of CRFs, outputs, SAPs)
Plan and manage submission activities, like SCS, SCE, briefing books.
Serve as a general clinical development and statistical resource at Agios; participate in non-clinical project activities
PhD in Biostatistics and 2+ years in biopharmaceutical industry as a biostatistician
MS Biostatistics and 6+ years in biopharmaceutical industry as a biostatistician
Fluent in English (oral and written)
Prior Experience with regulatory submissions
Proven knowledge and expertise in statistics and its applications to clinical trials
Fluent with statistical software including SAS, R, EAST, among others
Proven ability to work independently
Excellent communication and presentation skills
Team player, with ability to work successfully across functions
Innovative, flexible mindset