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We are using models early to fail less often, executing clinical trials to add valuation to the company, and generating fit-for-purpose data to feed back into Valos Opal Computational Platform as we reinvent drug discovery and development from the ground up.
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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.
$154,000 - $161,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Works with clinical or research departments to design, implement, and analyze studies for new medical equipment evaluations and trials. Under supervision and guidance, investigates clinical incidents involving medical devices and prepares and files appropriate reports (with department QA and Safety Coordinator), disseminates information regarding possible hazards and implements corrective action.
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Job Overview: This role will lead statistical analyses for early development of clinical trials, support investigators and researchers on experimental design, and collaborate closely with internal teams while reporting to the Head of Biometrics.
ExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Reporting to the Senior Director, Quantitative Sciences, the Manager of Programming, Statistics will be responsible for statistical programming activities across multiple studies and programs from study start-up through study closure to ensure completion per established project team goals and objectives.
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Serve as Medical Lead/Medical Monitor for assigned clinical trials/programs and ensure support of operational trial execution for Clinical Operations, Regulatory Affairs, Devices, Data Management, Statistics and other clinical trial team functions, with active participation on cross-functional development teams.
Full-timeExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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The Associate Director, Statistics is responsible for statistical and statistical programming activities across multiple studies and programs from study start-up through study closure to ensure completion per established project team goals and objectives.
Full-timeExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Accountable for operational excellence and timely production and approval of quality clinical deliverables, including clinical plans, protocols, clinical study reports and regulatory submission documents (e.g., NDA, MAA, AR, briefing documents, investigator’s brochures) and, working wih Medical Affairs, international meeting abstracts or manuscripts intended for external publication that are based on Pfizer-sponsored clinical trials.
$203,600 - $423,000 a yearFull-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Job Overview: The Senior Manager/Associate Director, Biostatistics will lead statistical analyses for early development of clinical trials, support investigators and researchers on experimental design, and collaborate closely with internal teams while reporting to the Head of Biometrics.
Full-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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Knowledge of clinical trials data processing concepts. Familiar with statistics and data analytics using SAS, SPSS, Stata, R, or Python COMPETENCIES. Clinical data processing/research/query creation/report writing.
Full-timeRemoteExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Bachelor’s or advanced degree in Statistics, Computer Science, Mathematics, or related field and 8-10+ years of experience as a SAS programmer working with clinical trial data in a pharmaceutical or biotech setting.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Familiarity with data management principles, regulatory requirements, and relevant guidelines for clinical trials and medical research. Lead biostatistician for Clinical Operations and Development, overseeing clinical study biostatistics deliverables.
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PhD in Statistics/Biostatistics preferred with exposure to clinical trials in pharmaceutical industry through internship or work experience. The Senior Statistician, Biostatistics provides statistical support for clinical trials, including but not limited to the following: contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards. BSc or MSc in Statistics, Mathematics, Computer Science or related subjects.
Full-timeExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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Lead M&S activities across all phases of development to support both regulatory filings and internal decision-makings by working closely across departments (i.e. DMPK, toxicology, biology, clinical, statistics etc,) and external vendors.
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