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Develop novel methodologies for analyzing immunological and pharmacokinetic data from both vaccine and monoclonal antibody clinical trials. Develop protocol scientific objectives and analytical laboratory testing plans for first-in-human clinical trials testing vaccines and therapeutics for infectious diseases.
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The Foundation for the National Institutes of Health (FNIH) is seeking a Program Manager for Translational Science, Cancer to manage a team and portfolio of large public-private research collaborations focused on identifying opportunities to validate and standardize assays, biomarkers and drug development tools for immune and other related oncology needs including patient centric clinical trials.
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The Biostatistics Center serves as the coordinating center for large scale multi-center clinical trials and epidemiological studies funded by federal agencies including the National Institutes of Health.
$66,433.08 - $106,155.95 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Participate in hands-on production in the manufacturing of material for clinical trials in a GMP environment, including operating expansion and production reactors, conducting harvest operations, and ordering and accounting for consumption of raw materials and components.
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With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
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PDS works with customers to develop new methods, validate existing methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials. Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development.
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Work closely with the Contracting Officer’s Representative (COR) to monitor, verify, and reconcile expenditure of budgeted funds supporting all clinical trials and other projects. We are seeking a Project Manager to potentially support the upcoming National Institutes on Deafness and Other Communication Disorders (NIDCD) Clinical Trials Program (CTP.
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The candidate will perform a variety of laboratory procedures and be familiar with the field's concepts, practices, and procedures, including, but not limited to, microbiology, immunology, vaccinology, biochemistry, genetics, molecular biology, clinical trials, and bioinformatics.
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Deep content knowledge and relationships in the field specific to cancer research and cancer clinical trials. Strong record of managing relationships among scientific and administrative partners from diverse sectors of biomedical science (e.g., government, academia, and/or private sector partners, industry, and not-for-profit organizations) with a desire to provide service excellence.
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We are seeking a Head of Process Engineering to join the Manufacturing, Science and Technology (MSAT) team and support ongoing process development, manufacturing of GMP grade material for company's Phase 1 and 2 clinical trials, technical transfer from preclinical to clinical Phase 2, IND authoring and agency interaction activities.
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Candidates are expected to have clinical research oversight expertise in mental health research with the ability to provide expert advice and consultation as needed on NIMH initiatives for clinical research studies and clinical trials including the scope, design, research study operations, human research protections and relevant federal regulation, data and safety monitoring, good clinical practive, and protocol compliance montoring.
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The Clinical Trials Administrator (CTA) Analyst reports into the Reporting and Compliance Team Lead and is responsible for handling the registration and monitoring of NCI Sponsored trials and facilitating the results reporting process associated with clinical trials reporting.
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At least 2 years of prior experience acting as a lead data manager in oncology clinical trials. Associate’s degree in the health sciences disciplines or related field of study and a minimum of 8 years of experience in the data management of clinical trials.
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PDS works with customers to develop new methods, validate existing methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials currently in different phases of the FDA regulated drug approval process.
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The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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clinical trials jobs in Rockville, MD
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