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The Director, Digital Quantitative Sciences is responsible for ensuring sound statistical thinking and methods are utilized in the discovery and development of novel digital and imaging endpoints and for bringing the principles of objective decision-making into the development, validation, and implementation of industry-leading digital health technology and imaging programs for incorporation into clinical trials across Pfizer’s portfolio.
$269,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Analyze, visualize and summarize NGS and other molecular data from oncology clinical trials and proprietary and public large molecular databases, including bulk tissue nucleotide acid sequencing and periphery comprehensive molecular assays including TCR sequencing, protein profiling, immune activation assays, and liquid biopsies.
$216,900 a yearFull-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Hands-on use of data science, machine learning and visualization to challenges faced in drug development including support for design and interpretation of clinical trials. We are a team of experts with a Machine Learning and Data Science backgrounds, solving problems for pharma and clinical trials.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Design clinical trials and calculate sample size for 2-by-2 crossover studies. Takeda Development Center Americas, Inc., is seeking a Manager, Statistics in Cambridge, MA with the following requirements: Master’s degree in Statistics, Biostatistics or related field or foreign academic equivalent plus 3 years of related experience.
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Alnylam US, Inc. seeks multiple Sr. Manager, Statistics in Cambridge, MA to collaborate with Clinical Development, Regulatory and Clinical Operations Expertise Areas to design clinical trials.
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Individuals with an MS (or equivalent) in Statistics, Biostatistics, or a closely related discipline (with formal statistical training) may be considered provided they have some post-graduate experience in clinical trials research in the pharmaceutical or a related industry and evidence of leading statistical methodology innovation.
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The role will work collaboratively across clinical teams to ensure strategy, planning, execution and data delivery of biomarker lab data for early and late phase infectious disease vaccine clinical trials conducted by Moderna.
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The Department of Biostatistics is comprised of approximately 30 faculty, who are internationally recognized for their innovation in research and scholarship in a diverse range of areas of biostatistics including statistical genetics, clinical trials, surveillance, longitudinal studies, Bayesian statistics and risk prediction.
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Several years of relevant experience in immuno-oncology, oncology and/or infectious diseases in a biotech/pharmaceutical and/or academic environment, including leadership of clinical development activities, ideally from exploratory Phase I/II clinical trials through late stage development in Phase III and NDA submission.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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We are actively engaged in several clinical trials, pharmacoepidemiology, chronic disease epidemiology, genetic epidemiology, biostatistical and genomics research. Observational study or clinical trials research and analysis experience.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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This position will manage all statistical activities including statistical programming from CRF design through clinical study report for in-house and outsourced clinical trials with minimal supervision.
Full-timeExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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Experience in applied statistics and/or biostatistics related to the design and analysis of biomedical/clinical trials. Evaluating design and execution of preclinical and clinical trials.
$190,900 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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PhD/MS in statistics or related discipline with at least 7 (9 for MS) years of clinical development experience in pharma/biotech industry and should have at least 4 years of leading experience in development of digital biomarkers (establishing a novel digital biomarker or digital COA or ePRO in clinical trials.
Full-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Responsibilities include managing all statistical activities from CRF design through clinical study report for in-house and outsourced clinical trials with minimal supervision. The Programming and Statistics Manager will manage statistical programming activities across multiple studies and programs from study start-up through study closure.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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This position requires strategic agility, knowledge of clinical trials, strong project management and communication skills, an interest in writing manuscripts and grants, and interaction with multiple faculty and staff members across the Harvard-wide community.
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