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Following the Ph. D., 2+ years of mathematical modeling & computer simulation experience in the pharmaceutical industry for the Sr. Research Investigator level. No additional industry experience is needed for the Research Investigator level.
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The Clinical Research Coordinator (CRC) will independently, or with general direction, execute, manage, and coordinate clinical research protocols, as directed by the Lead Clinical Research Coordinator, Principal Investigator (PI), and/or the Research Personnel Director for the Breast Oncology program.
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These services consist of several functional areas housed within the HDFCCC, including the DSMC, Clinical Research Support Office (CRSO), Clinical Research Network Office (CRNO) and the Protocol Review and Monitoring Committee (PRMC), with oversight from the Cancer Center Clinical Research Oversight Committee (CCCROC.
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Following the Ph. D., 2+ years of mathematical modeling & computer simulation experience in the pharmaceutical industry for the Sr. Research Investigator level or 5+ years for the Associate Director level.
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In addition to the financial oversight of Principal Investigator (PI) portfolios, this position also provides financial oversight for the American Course on Drug Development and Regulatory Sciences (ACDRS) Program, the Bioengineering Graduate Program, the Clinical Pharmacology Training Program (CPT), the Master of Translational Medicine degree program (MTM), and the Pharmacokinetics for Pharmaceutical Scientists (PK Course.
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The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI; Dr. Martinez); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
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Serves as an internal and external resource for questions referencing clinical research at NCH. · Professionally represents Principal Investigator and NCH Research Institute at protocol meetings and conference calls in the absence of the Investigator.
$10,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We currently have a position for a Research Associate located at Walter Reed Army Institute of Research in Silver Spring, MD. This position will be supporting Shigella vaccine development.
$50 - $65 an hourFull-timeRemoteExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Understanding of the related disciplines (i.e. biostatistics, regulatory, pharmacology and toxicology research, cell therapy manufacturing, clinical pharmacology and pharmaceutical sciences.
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Experience with clinical biospecimen testing, assay development, and bioanalytical method qualification. The successful candidate will conduct laboratory activities related to ongoing and future cell therapy clinical studies in rheumatology or neurology indications.
$85,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Oversight of database lock activities and ultimate archiving of study data 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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The work environment is a biomedical research laboratory. This position is training under Principal Investigator. Assist with training of research methods and approaches to laboratory group.
$66,560 - $79,639.96 a yearFull-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Compliance with company and local IACUC/AAALAC regulations for animal research. Data collection including subcutaneous tumor measurements (caliper), body weight measurement, and clinical/animal health observations.
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Quantitative Systems Pharmacology (QSP) & Physiologically Based Pharmacokinetics (PBPK) have become important components of discovery and clinical development. + Desire to interact as a modeling and simulation expert with matrix project teams and working closely with experts from different functional areas (pre-clinical and clinical and multiple therapeutic areas.
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Minimum of 10 years of working in clinical research and drug development in the pharmaceutical industry (and/or Contract Research Organizations) with specific experience with TMF, clinical documentation and/or records & information management.
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clinical research investigator jobs Title: senior clinical research coordinator Company: Hp in San Francisco, CA
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