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Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials.
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Scope of work will include tasks associated with the execution, monitoring, and reporting of late-phase clinical trials evaluating therapeutics in immune-mediated dermatologic, gastrointestinal, rheumatologic diseases, or rare diseases.
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JOB DESCRIPTION Description:Manages multiple investigator-initiated clinical trials. Builds research infrastructure to support multi-center clinical trials. Oversees and drives projects from concept to final deliverables in form of publications, clinical study reports, final reports to funding agency, etc.
$100,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Each ENT and Allergy Associates clinical location provides access to a full complement of services, including General Adult and Pediatric ENT, Voice and Swallowing, Facial Plastics and Reconstructive Surgery, Disorders of the Inner Ear and Dizziness, Asthma, Clinical Immunology, Diagnostic Audiology, Hearing Aid dispensing, Sleep and CT Services as well as advanced Immunodeficiency trials.
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This role plays a pivotal role in coordinating and overseeing clinical operations of all assigned Clinical Research Nurse and Clinical Trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research studies.
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Execute sample testing and analysis for toxicology and clinical trials. Provide critical data review of clinical and non-clinical data. Perform the biofunctional immunological assays to support vaccine clinical development in a high-throughput setting.
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Perform integrative analyses of multi-omics data from clinical trials and research cohorts, including genomics, transcriptomics, proteomics, and imaging, to identify biomarkers related to treatment mechanism and response, and potential therapeutic targets.
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The Field Service Engineer is responsible for providing on-site support to BD customers that includes, but is not limited to: installation and service of diagnostic instrumentation, after-hours phone support, holiday and weekend on-site support, marketing, exhibitions, and clinical trials support.
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Flow Cytometry experience is a plus. Prior Field Service Engineer experience. Report quality control and other technical problems, in detail, to the Service Center and System Support Engineering Manager.
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PDI is seeking a Clinical Scientist II - Microbiology to conduct antimicrobial testing, method development, and develop the strategy, design, execution, and interpretation of clinical trials in support of early drug development.
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You will drive activities around computer programming, system administration, and support of computer systems used within clinical testing operations. Weekend/night work required on occasion when coordinating off hour system upgrades or weekend end-user support.
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Massive Bio is a rapidly growing health-tech startup founded in 2015 to provide every cancer patient with access to clinical trials regardless of their location or financial stability. Our proprietary patient recruitment and enrollment enablement solution for oncology clinical trials solves every point of friction in traditional clinical trial enrollment.
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Doctorate (Ph. D.) in Public Health, Statistics, Data Science, or a discipline relevant to clinical trials, or PharmD. As part of our purpose to achieve "breakthroughs that change patients' lives", Pfizer is creating a new Pragmatic Clinical Trials Center of Excellence (PCT-CoE) within the Worldwide Medical & Safety (WMS) organization.
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Develop and/or review statistical documents and deliverables for clinical trials including Statistical Analysis Plan (SAP) for individual studies and integrated summaries of drug efficacy and safety, Table, Listing and Graph (TLG) shells, statistical validation plan, Data Set Specification (Rule Book), Data Monitoring Committee Charter and interim analysis plan, Clinical Study Report (CSR) and others.
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clinical trials jobs in Woodcliff Lake, NJ
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