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Master’s degree or Ph. D. in a quantitative discipline such as mathematics, statistics, biostatistics, computer science, bioinformatics, or computational biology. The company’s platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs.
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Proclinical Staffing is seeking an Associate Director Biostatistics to join a cutting-edge pharmaceutical company. The Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.
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Advanced degree in Epidemiology/Biostatistics or 2+ years of epidemiological research in a health care, pharmaceutical, or health-related academic field. Experienced conducting studies with medical coding sets (e.g. HCPCS, ICD, CPT, SNOMED, LOINC, and NDC.
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PhD (8+ years) or MS (10+ years) in statistics or biostatistics or related scientific field with experience in clinical trials in the pharmaceutical or biotechnology industry. The Director, Biostatistics is a member of a cross-functional product development team and contributes to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions.
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Collaborates with Clinical Operations, Data Management, Clinical Development, Drug Safety, Statistical Programming, and Biostatistics to develop standard and custom data reports for quality data oversight / clinical data review.
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PhD in Computational Biology, Systems Biology, Immunology, Molecular Biology, Biostatistics, Bioengineering, or similar; or equivalent professional experience. PhD in Computational Biology, Systems Biology, Immunology, Molecular Biology, Biostatistics, Bioengineering, or similar; or equivalent professional experience.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Strong working knowledge and/or interest in database management, biostatistics, bioinformatics, systematic reviews, metabolomics preferred. Identify and actively participate in relevant short courses, workshops, and seminars for further training (e.g., systematic reviews, biosafety, mass spectrometry) that is complementary to the postdoctoral fellow’s background and necessary for successful study execution.
$64,500 - $70,000 a yearFull-timeExpandUpdated 4 days ago - UpvoteDownvoteShare Job
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Lead and manage external (and/or internal) biostatistics and statistical programming resources supporting studies and programs. He/She is also accountable for the production of biostatistics deliverables by providing oversight of the work performed by CROs, managing external (and/or internal) biostatistics and statistical programming resources, or performing the work themselves.
$220,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Collaborate with internal and external partners, including Biostatistics, Statistical Programming, Clinical Operations, Clinical Research, Quality Assurance, Global Patient Safety and Risk Management, and Regulatory Affairs; CROs, central and local laboratories, and other vendors.
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Experience working with Medidata Rave. Experience using standardized medical terminology, including MedDRA and WHODrug. Collaborate with Statistical Programming to oversee SDTM validation efforts, performing review of validation reports, SDTM Reviewer Guides and define.
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Firmly grounded in the scientific fundamentals of one or more of the core HEOR specialties (epidemiology, biostatistics, patient reported outcomes, health services research, economics, clinical practice or behavioral science.
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G., Clinical Operations, Clinical Development, Biostatistics and Data Management, Pharmacovigilance, etc.) Experience working effectively with CROs/CSPs. Expe rience with electronic Quality Management Systems and Trial Master File. Skills and Abilities A solid understanding of GCP, GLP, GMPs and CMC requirements is expected.
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This position will work in close partnership with colleagues in Clinical Pharmacology, Biostatistics, Nonclinical Development, Bioanalysis, and Biometrics, as well as with external vendors and partners creating an aligned, quantitative framework to impact strategies and decisions on drug development.
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Leveraging cutting-edge advancements in molecular visualization, computational chemistry, and data integration, our client develops orally available, superior small molecule medicines targeting chronic diseases with significant unmet needs such as cardiovascular, metabolic, and pulmonary conditions.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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We are seeking an exceptional Senior Principal Statistician with strong statistical and computational skills to support multiple complex clinical trials in Oncology and COVID. The Senior Principal Statistician is responsible for leading and performing biostatistics and statistical programming activities in these trials, which may be Phase I, II and III pharmaceutical trials and medical device trials evaluating new biomarkers and/or therapeutics.
ExpandApply NowActive JobUpdated 10 days ago
biostatistics job in South San Francisco, CA
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